BITS Pilani

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Publications

Complete list of Research Articles (More than 550)

  • COVID-19: vaccines and therapeutics, Ponnampalli, S.; Birudukota, N.V.S.; Kamal, A., Bioorg. Med. Chem. Lett. 2022, (in press).
  • Novel approaches to the development of direct KRAS inhibitors: Structural insight and drug design. Sharma, A.; Yakkala, P.A.; Yar, M.S.; Shafi, S.; Kamal, A., Expert Opinion on Drug Discovery, 2022, 17, 247.
  • Novel linezolid-based oxazolidinones as potent anticandidiasis and antitubercular agents Faazil, S.; Malik, M.S.; Ahmed, S.A.; Alsantali, R.I.; Yedla, P.; Alsharif, M.A.; Shaikh, I.N.; Kamal, A., Bioorg. Chem. 2022, 126, 105869.
  • Synthesis and characterization of novel combretastatin analogues of 1,1 diaryl vinyl sulfones, with antiproliferative potential via in silico and in vitro studies. Egharevba, G.; Kamal, A.; Dosumu, O.; Routhu S.; Fadare O.; Oguntoye S.; Njinga S.; Oluyori, A., Scientific Reports., 2022, 12, 1901.
  • Stereoselective synthesis of (Z)-1,3-bis (α,β-unsaturated carbonyl)-isoindolines fromaldehydes and phenacyl azides under metal free conditions. Prasad, B.; Phanindrudu, M.; Nanubolu, J.B.; Kamal, A; Tiwari, D.K., Chem. Commun., 2021, 57, 9542.
  • Identification, characterization and evaluation of novel antifungal cyclic peptides from Neobacillus drentensis. Routhu, S.R.; Ragi, N.C.; Yedla, P.; Shaik, A.B.; Venkataraman, G.; Chandrasekhar, C.; Kumar, C.G.; Amanchy, R.; Sripadi, P.; Kamal, A., Bioorg. Chem., 2021, 115, 105180.
  • New indenopyrazole linked oxadiazole conjugates as anti-pancreatic cancer agents: Design, synthesis, in silico studies including 3D-QSAR analysis. Khan, I.; Ganpathi, T.; Rehman, M.M; Shareef, M.A.; Kumar, G.; Kamal, A., Bioorg. Med Chem. Lett., 2021, 44, 128094.
  • β-Carbolines as potential anticancer agents. Aaghaz, S.; Sharma, K.; Jain, R.; Kamal, A., Eur. J. Med. Chem., 2021, 216, 113321. 
  • In-silico driven design and development of spirobenzimidazo-quinazolines as potential DNA gyrase inhibitors. Korrapati Suresh Babu S.K., Yedla P., Pillai G.G, Mohammad F, Reddy V.R., Bhamidipati P., Amanchy R, Syed R., Kamal A., Biomed. Pharmacol., 2021, 134, 111132.
  • Identification and characterization of in vitro and in vivo fiderestat metabolities: Toxicity and efficacy evaluation of metrobolites. Borkar, R.M.; Gajji, S.; Mohammed, S.A.; Srivastava, M; Reddy, C.G.; Jala, A; Asthana, S.; Kamal, A., Banerjee, S.K., J. Mass Spectrometry, 2021 (2021, 56,e4694).
  • Synthesis, biological evaluation, and molecular docking analysis of phenstatin based indole linked chalcones as anticancer agents and tubulin polymerization inhibitors. Kode, J.; Kovvuri, J.; Nagaraju, B.; Jadhav, S.; Barkume, M.; Sen, S.; Kasinathan, N.K., Chaudhari, P., Mohanty, B.S.; Gour, J.; Sigalapalli, D.K.,; Kumar, C.G.; Pradhan, T.; Banerjee, M.; Kamal, A., Bioorg. Chem., 2020, 105,104447.
  • New imidazo[2,1-b]thiazole-based aryl hydrazones: unravelling their synthesis and antiproliferative and apoptosis-inducing potential. Shareef, M. A.; Devi, G. P.; Routhu, S.R.;  Kumar, C.G.; Kamal, A., Babu, B.N.; RSC Med.Chem. 2020, 11, 1178.  
  • Base-mediated 1,3-dipolar cycloaddition of pyridinium bromides with bromoallyl sulfones: A facile access to indolizine scaffolds. Jadala C.;  Reddy, V.G.; Harikrishna N.; Shankariah, N; Kamal, A., Org. Biomol. Chem., 2020, 18, 8694.
  • Synthesis and biological evaluation of substituted N-(2-(1H-benzo[d]imidazol-2-yl)phenyl)cinnamides as tubulin polymerization inhibitors. Donthiboina, K.; Anchi, P.; Gurram, S.; Mani, G, S.; Uppa, J. L., Godugu, C.; Shankariah, N; Kamal, A., Bioorg. Chem., 2020, 103, 104191.
  • Synthesis of (Z)-3-(arylamino)-1-(3-phenylimidazo[1,5-a]pyridin-1-yl)prop-2-en-1-ones as potential cytotoxic agents. Mani, G, S.; Anchi, P.; Sunkari, S; Donthiboina, K.; Godugu, C.; Shankaraiah, N.; Kamal, A., Bioorg. Med. Chem. Lett., 2020, 30, 127432.
  • Discovery of Novel Tankyrase Inhibitors through Molecular Docking-based Virtual Screening and Molecular Dynamics simulation Studies. Palyulin,V,A.;  Berishvili,V.P.; Kuimov, A.N.; Voronkov, A.E., Radchenko, E.V.; Kumar, P.; Choonara,Y. E.; Pillay,V.; Kamal, A., Molecules, 2020, 25, 3171. 
  • Design and Synthesis of 5-Morpholino-Thiophene-Indole/Oxindole Hybrids as Cytotoxic Agents. Yadav, U.; Sakla, A.P; Tokala, R.; Nyalam, S. T.; Khurana, A; Digwal, C.S.; Talla, V.; Godugu, C.; Shankaraiah, N.; Kamal, A., Chemistry Select, 2020, 5, 4356. 
  • Amberlite IR-120H Catalyzed Synthesis of 1,3-Diphenylpyrazole-chromenoquinolin-6-one Compounds and Their Biological Evaluation.  Kovvuri, J.; Nagaraju, B.;  Kumar, C.G.; Routhu, S.R.; Gour, J.; Mullagiri, K.; Nagesh, N.; Kamal, A., American Journal of Medicinal Chemistry, 2020 (in press).
  • Iodine-mediated oxidative annulation by C─C cleavage: A domino synthetic approach to quinazolinones and benzo[4,5]imidazo[1,2-c]quinazolines. Donthiboina, K.; Mani, G, S.; Shankaraiah, N.; Kamal, A., Chemistry Select, 2020, 5, 3923.
  • Synthetic Lethality on Drug Discovery: an update on Cancer Therapy. Yar, M.S.; Haider, K.; Gohel, V.; Siddiqui, N.A.; Kamal, A., Expert Opinion on Drug Discovery, 2020, 15, 823.
  • A Comprehensive Review on the Therapeutic Versatility of Imidazo[2,1-b]-thiazoles. Shareef, M. A.; Khan, I.; Babu, B.N.; Kamal, A., Current Medicinal Chemistry, 2020,27,6864.
  • Application of triazoles as bioisoteres and linkers in the development of microtubule targeting agents. Malik, M. S.; Ahmed, S.A.; Seddigi, Z. S.; Ansari, M. A.; Kamal, A., RSC Med.Chem. 2020, 11, 327.
  • Evaluation of anticancer and anti-mitotic properties of quinazoline and quinazolino-benzothiadiazine derivaties. Thoukhir, B.S.; Kamal, A.; Malik, M. S.; Routhu, S.R.; Seddigi, Z.S.; Althagafi, I. I, Anti Cancer Agents Med.Chem., 2020, 29,599.
  • Hypervalent iodine (III) catalyzed rapid and efficient access to benzimidazoles, benzothiazoles and quinoxalines: Biological evaluation of some new benzimidazole-imidazo[1,2-a]pyridine conjugates. Ramya, P.V.S.; Angapelly, S.; Rani, R.S.; Digwal, C.S.; Kumar, C.G.; Babu, B.N.; Guntuku, L; Kamal, A.,  Arabian J. Chem., 2020, 13, 120.
  • Efficient and green sulfamic acid catalyzed synthesis of new 1,2-dihydroquinazoline derivatives with antibacterial potential. Kamal, A.; Babu, K.S.; Poornachandra, Y.; Nagaraju, B.; Hussaini, S.M.A; Shaik S. P.; Kumar, C.G.; Alarifi, A., Arabian J. Chem. 2019, 12, 3546.
  • Arylcinnamido-propionone conjugates as tubulin polymerization inhibitors and apoptotic inducers. Rao, N.S; Nayak,V.L; Rao, AV.S; Hussaini, S.M.A; Sunkari, S; Alarifi, A; Kamal, A., Arabian J. Chem., 2019, 12, 4740.
  • Synthesis of combretastatin-A4 carboxamides that mimicsulfonyl piperazines by a molecular hybridization approach: in vitro cytotoxicity evaluation andinhabitation of tubulin polymerization.  Jadala C.; Sathish, M; Anchi, P.; Tokala, R.; Lakshmi, U.J.; Ganga, R.; Shankaraiah, N.; Godugu, C.; Kamal, A., ChemMedChem., 2019, 14, 2052.
  • Transition metal-free one-pot synthesis of substituted pyrroles by employing aza-wittig reaction. Jadala, C; Prasad, B; Prashant, A.V.G.; Shankaraiah, N; Kamal, A, RSC Adv., 2019, 9, 30659.
  • Transition metal free one-pot tandem synthesis of 3-Ketoisoquinolines from aldehydes and phenacyl azides. Prasad, B.; Phanindrudu, M; Tiwari, D.K.; Kamal, A, J. Org. Chem., 2019, 84, 12334.
  • Iodine-promoted one-pot synthesis of 1,3,4-oxadiazole scaffolds via sp3 C-H functionalization of azaarenes. Mani, G, S.; Donthiboina, K.; Shankaraiah, N.; Kamal, A., New J. Chem., 2019, 43, 15999.
  • Iodine-mediated C–N and N–N bond formation: a facile one-pot synthetic approach to 1,2,3-triazoles under metal-free and azide-free conditions. Mani, G, S, Donthiboina, K; S Shaik S. P.; Shankaraiah, N.; Kamal, A., RSC Adv., 2019, 9, 27021.
  • Synthesis of new triazole fused imidazo[2,1-b]thiazole hybrids with emphasis on staphylococcus aureus virulence factors. Shareef, M.A.; Sirisha, K.; Sayeed, I. B.; Khan, I.; Ganapathi, T.; Akbar, S.; Kumar, C.G.; Kamal, A.; Babu, B.N., Bioorg. Med. Chem. Lett., 2019, 29, 126621.
  • Design and synthesis of 4β-Acetamidobenzofuranone-podophyllotoxin hybrids and their anti-cancer evaluation. Paidakula, S.; Nerella, S.; Vadde, R.; Kamal, A.; Kankala, S., Bioorg. Med. Chem. Lett., 2019, 29, 2153.
  • Tubulin inhibitors as novel anticancer agents: an overview on patents (2013-2018). Haider, K.; Rahaman, S; Yar, M.S.; Kamal, A.; Expert Opinion on Therapeutic Patents, 2019, 29, 623.
  • Combretastatin based compounds with therapeutic characteristics: a patent review.  Nainwal, L.M., Alam, M. M., Shaquiquzzaman, M.; Marella, A.; Kamal, A., Expert Opinion on Therapeutic Patents, 2019, 29, 703.
  • Pyrazolo-benzothiazole hybrids: Synthesis and evlatuion of anticancer properties with VEGFR-2 Kinase inhibition and anti-angiogenesis in transgenic zebrafish in vivo model. Reddy, V.G.; Reddy, T, S.; Jadala, C.; Reddy, M.S.; Sultana, F.; Akunri, R.; Bhargava, S, K.; Wlodkowic, D.; Srihari, P.; Kamal, A., Eur. J. Med. Chem., 2019, 182, 111609.
  • Time-Domain analysis of molecular dynamics trajectories using deep neural networks: application to activity ranking of tankyrase inhibitors. Berishvili, V. P.; Perkin, V.O.; Voronkov, A., E; Radchenko, E.V.; Riyaz, S.; Reddy, V, R., C; Pillay, V.; Kumar, P.; Choonara Y, E.;  Kamal, A.; Palyulin, V, A.;  J. Chem. Inf. Model, 2019, 59, 3519.
  • Styryl Quinazolinones and its ethynyl derivatives induce myeloid differentiation.  Radhakrishnan, S.; Syed, R.;  Takei, H.; Kobayashi, I. S.; Nakamura, E.;  Sultana, F.; Kamal, A.; Tenen, D,G.; Kobayashi, S. S., Bioorg. & Med. Chem., 2019, 29, 2286.
  • Synthesis and in vitro cytotoxicity evaluation of β-carboline-combretastatin carboxamides as apoptosis inducing agents: DNA intercalation and topoisomerase-II inhibition. Jadala, C.; Sathish M.; Reddy T. S.; Tokala, R.; Bhargava S.K.;Shankaraiah, N.; Nagesh, N.;Kamal, A., Bioorg. & Med. Chem., 2019, 27, 3285.
  • Synthesis of 2-anilinopyridyl linked benzothiazole hydrazones as apoptosis including cytotoxic agents.  Sultana, F.; Saifi, M. A.; Syed R.; Mani, G. S.; Shaik S. P.; Osas, E. G.; Godugu, C.; Shahjahan, S.; Kamal, A., New J. Chem., 2019, 43, 7150.
  • Synthesis and biological evaluation of new bisindole-imidazopyridine hybirds as apotosis inducers.  Sunkari, S.; Bonam S. R.; Rao, A.V.S.; Riyaz, S.; Nayak, V. L.; Kumar, H.M.S.; Kamal, A.;  Babu, B.N., Bioorg. Chem., 2019, 87, 484.
  • Synthesis and biological evaluation of phenyl-amino-pyrimidne and indole/oxindole conjugates as potential BCR-ABL inhibitors. Rahim A.; Syed, R.; Poornachandra, Y.; Malik, M. S.; Reddy, Ch. R.; Alvala, M.; Boppana, K.; Sridhar B.; Amancy, R.; Kamal, A., Medicinal Chemistry Research, 2019, 28, 633. 
  • Synthesis of benzo[d]imidazo[2,1-b]thiazole-propenone conjugates as cytotoxic and apoptotic inducing agents. Shaik, S.P.; Reddy T. S.; Sunkari, S.; Rao, A.V.S.; Babu, K.S.; Bhargava S.K.; Kamal, A., Anti-Cancer Agents in Medicinal Chemistry, 2019, 19. 
  • One pot synthesis and biological evalution of arylopropenone aminochalcone conjugates as potential apoptic inducers. Khan, I.; Ganapathi, T.; Shareef, M.A.; Shaik, A.B.; Akbar, S.; Ranjanna, A.; Kamal, A.; Kumar, C.G., Chemistry Select, 2019,4, 4672.
  • Design, synthesis and antimicrobial evaluation of 1,4-dihydroindeno[1,2-c]pyrazole tethered carbohydrazide hybrids: Exploring their in silico ADMET, antibiofilm, ergosterol inhibition and ROS inducing potential. Shareef, M.A.; Sirisha, K.; Khan, I.; Sayeed, I. B.; Gopathi, R.; Kumar, C.G.; Kamal A.; Bathini, N. B., MedChemCommun., 2019, 10, 806.
  • Synthesis of new bis-pyrazole linked hydrazides and their in vitro evaluation as antimicrobial and anti-biofilm agents: A mechanistic role on ergosterol biosynthesis inhibition in Candida albicans. Khan, I.; Sirisha, K.; Shareef, M.A.; Ganapathi,T.; Shaik, A.B.; Shekar, K.C.; Kamal, A.; Kumar, C.G., Chem.Biol. & Drug Design, 2019, 94, 1339. 
  • Synthesis and biological evaluation of pyrazole linked benzothiazole-β-naphthol derivatives as topoisomerase I inhibitors with DNA binding ability.  Nagaraju, B.; Kovvuri,J.; Kumar, C.G.; Routhu, S.R.; Shareef, M.A.; Kadagathur, M.; Adiyala, P.R.; Alavala, S.; Nagesh, N.; Kamal, A.; Bioorg. & Med. Chem., 2019, 27, 708. 
  • Induction of apoptosis in lung carcinoma cells by antiproliferative cyclic lipopeptides from marine algicolous isolate Bacillus atrophaeus strain AKLSR1.Routhu, S.R; Chary, R.N.; Shaik, A.B.; Prabhakar, S.; Kumar, C.G.; Kamal, A.; Process Biochemistry, 2019, 79, 142.
  • Design, synthesis and biological evaluation of substituted (1-(4-chlorobenzyl)-1H-indol-3-yl) 1H-(1,2,3-triazol-4-yl) methanones as antifungal agents. Shareef, M.A.; Rajpurohit, H.; Sirisha, K.; Sayeed, I.B.; Khan, I; Kadagathur, M.; Ganapathi, T.; Kumar, C.G.;Kamal, A.; Babu, B.N.;Chemistry Select, 2019, 4, 2258.
  • Design, synthesis, in silico pharmacokinetics prediction and biological evaluation of 1,4-dihydroindeno[1,2-c]pyrazole chalcone as EGFR/Akt pathway inhibitors. Khan, I.; Garikapati, K.R.; Setti, A.; Shaik, A.B.; Makani, V.K.K.; Shareef, M.A.; Rajpurohit, H.; Vangara, N.; Pal-Bhadra., M; Kamal, A.; Kumar, C.G.,  Eur.J. Med. Chem., 2019, 163, 636.
  • Synthesis of substituted biphenyl methylene indolinones as apoptosis inducers and tublin polymerization inhibitors. Donthiboina, K.; Anchi, P.; Ramya, P.V.S.; Karri, S.; Srinivasulu, G.; Godugu, C.; Shankaraiah, N.; Kamal, A.; Bioorg. Chem., 2019, 86, 210.
  • Multicomponent access to novel proline/cyclized cysteine tethered monastrol conjugates as potential anticaner agents. Malik, M.S.; Seddigi, Z.S.; Bajee, S.; Azeeza, S.; Riyaz, S.; Ahmed, S.A.; Althagafi, I. I.; Jamal, Q.M.S.; Kamal, A., J. Saudi Chem. Soc., 2019, 23, 503.
  • Peptides as potential anticancer agents.  Aaghaz, S.; Gohel, V.; Kamal, A., Curr. Top. Med. Chem., 2019, 19, 1491.
  • Synthesis and biological evaluation of 1-benzyl-N-(2-(phenylamino)pyridin-3-yl)-1H-1,2,3-triazole-4-carboxamides as antimitotic agents.  Prasad, B.; Nayak, V.L.; Srikanth, P.S.; Baig, M, F.; Subba Reddy, N.V.; Babu, K.S.; Kamal, A., Bioorg. Chem., 2019, 83, 535.  
  • Design and synthesis of DNA-intercalative naphthalimide-benzothiazole/cinnamide derivates: Cytotoxicity evaluation and topoisomerase-IIα inhibition. Kamal, A.; Shankaraiah, N.; Regur, P.; Gaddam, K.; Tokala, R.; Sunkari, S.; Nayak, V.L.; Nagesh, N.;  Rao, N.S.; Med. Chem. Comm., 2019, 10, 72.
  • Zinc Dependent Histone Deacetylase Inhibitors in Cancer Therapeutics: Recent Update. Sultana, F; Manasa, K. L.; Shaik, S.P.; Bonam S. R; Kamal, A., Curr. Med. Chem., 2019, 26, 7212.
  • Styryl Quinazolinones as potential inducers of Myeloid Differentiation via Upregulation of C/EBPα.  Sridhar, R.; Takei, H.; Riyaz, S.; Kobayashi, I.S.; Hui, L.B.; Kamal, A., Tenen, D.G.; Kobayashi, S.S., Molecules, 2018, 23, 1938.
  • 1(3)-Formyl-b-carbolines: Potential Aldo-X Precursors for the Synthesis of b-Carboline-Based Molecular Architectures. Devi, N; Kumar, S; Pandey, S. K.; Singh, V.; Asian J. Org. Chem., 2018, 7, 6.
  • Regioselective Ring Expansion of Isatins with In Situ Generated α-Aryldiazomethanes: Director Access to Viridicatin Alkaloids. Tangella, Y.; Manasa, K.L.; Harikrishna, N.; Sridhar B.; Kamal, A.; Babu, B.N., Org. Lett., 2018, 20, 3639.
  • Sulfamic acid promoted one-pot synthesis of phenanthrene fuseddihydrodibenzo-quinolinones: Anticancer activity, tubulin polymerization inhibition and apoptosis inducing studies. Kumar, N. P.; Kumari, S.S.; Lakshmi, U.J.; Tokala, R.; Shankaraiah, N.; Kamal, A., Bioorg. Med. Chem., 2018, 26, 1996.
  • Imidazopyridine linked triazoles as tubulin inhibitors, effectively triggering apoptosis in lung cancer cell line. Sayeed, I.B.; Vishnuvardhana, M.V.P.S.; Nagarajan, A.; Kantevari, S.; Kamal, A., Bioorg. Chem., 2018, 80, 714.
  • Synthesis of enamino-2-oxindoles via conjugate addition between α-azido ketones and 3-alkenyl oxindoles: Cytotoxicity evaluation and apoptosis inducing studies.  Kumara N. P.; Vanjaria, Y., Thatikondab, S.; Pooladandab V., Sharma P.; Sridhard B.; Godugub,C.; Kamal, A.; Nagula S.; Bioorg. Med. Chem. Lett., 2018, 28, 3564.
  • Synthesis of DNA interactive C3-trans-cinnamide linked β-carboline conjugates as potential cytotoxic and DNA topoisomerase I inhibitors. Thatikonda, S.; Tangella, Y.; Krishna, H.; Nekkanti, S.; Dushantrao, S.C.; Cherukommu, S.; Srinivas, G.; Tokala, R.; Nagesh, N.; Manda, S.; Nagula S.; Kamal, A., Bioorg. Med. Chem. Lett., 2018, 26, 4916.
  • Molecular idone-catalysed oxidative CO-C(alkyl) bond cleavage of aryl/heteroaryl alkyl ketones: An efficient strategy to access fused polyheterocycles. Shankaraiah N.; Namballa, H.R.; Sultana, F.; Sunkari, S.; Tangella Y.; Subba, R.A.V.; Mani, S.G.; Kamal, A., New J.Chem., 2018, 42, 15820.
  • Vanadium-catalyzed  N-benzoylation  of   2-aminopyridines    via oxidative C(CO)–C(CO)  bond  cleavage of 1, 2-diketones, N→N' aroyl migration   and  hydrolysisof 2-(diaroylamino) pyridines. Digwal, C.S.; Yadav, U.; Ramya, P.V.S.; Swain, B.; Kamal, A., Asian J. Org. Chem., 2018, 7, 865.
  • Synthesis and biological evaluation of curcumin inspired imidazo[1,2-a]pyridine analogues as tubulin polymerization Inhibitors. Ramya, P.V.S.; Guntuku L.; Angapelly S.; Digwal C.S.; Lakshmi, U.J.; Sigalapalli, D.K.J.; Babu, B.N.; Naidu V.G.M.; Kamal, A., Eur. J. Med. Chem., 2018, 143, 216.
  • Microwave-assisted one-pot synthesis of new phenanthrene fused-tetrahydrodibenzo-acridinones as potential cytotoxic and apoptosis inducing agents. Kumar,N.P.; SharmaP.;ReddyT. S.;Shankaraiah N.; Bhargava S.K.;  Kamal,A., Eur. J. Med. Chem., 2018, 151, 173.
  • Curcumin inspired 2-chloro/phenoxy quinolone analogues: Synthesis and biological evaluation as potential anticancer agents. Ramya, P.V.S.; Lalita G.; Srinivas, A.; Shailaja, K.; Digwal C.S.; Babu B.N.; Naidu, V.G.M.; Kamal, A., Bioorg. Med. Chem. Lett., 2018, 28, 892.
  • Synthesis and biological evalutation of imidazo[2,1-b]thiazole-benzimidazole conjugates as microtubule-trageting agents. Baig M.F.; Nayak V.L.; Prasad B.; Kishore M.; Satish S.; Gour J.; Kamal, A., Bioorg. Chem., 2018, 77, 515.
  • Iodine promoted dual oxidative C(sp3)-H amination of 2-methyl-3-arylquinazoline-4(3H)-ones; a facile route to 1, 4-dairylimidazo[1,5-a]quinazolin-5(4H)-ones. Kavita D.; Harikrishna N.; Shaik S.P.; Nanubolu J.B.; Shankaraiah N.; Kamal, A., Org. Biomol. Chem., 2018, 16, 1720.
  • Iodine mediated oxidative cross-coupling of unprotected anilines and heteroarylation of benzothiazoles with 2-methylquinoline. Rahim A; Shaik S. P.; Baig M.F.; Alarifi A.; Kamal, A., Org. Biomol. Chem., 2018, 16, 635
  • Synthesis of podophyllotoxin linked β-carboline congeners as potential anticancer agents and DNA topoisomerase II inhibitors. Sathish M.; Kavitha B.; Nayak V.L.; Tangella Y.; Ajitha A.; Nekkanti S.; Alarifi A.; Shankaraiah N.; Nagesh N.; Kamal, A., Eur. J. Med. Chem., 2018, 144, 557.
  • 4β-Amidotriazole linked podophyllotoxin congeners: DNA topoisomerase-IIα inhibition and potential anticancer agents for prostate cancer. Reddy, V.G.; Bonam, S.R.; Reddy, T.S.; Akunuri, R.; Naidu, V.G.M.;  Nayak, V.L.; Bhargava, S.K.; Kumar, H.M.S.; Srihari, P.; Kamal, A.,  Eur. J. Med. Chem., 2018, 144, 595.
  • New (3-(1H-benzo[d]imidazol-2-yl)/(3-(3H-imidazo[4,5-b]pyridin-2-yl)-(1H-indol-5-yl)(3,4,5-trimethoxyphenyl)methanone conjugates as tubulin polymerization inhibitors. Mullagiri, K.; Nayak V.L.; Satish, S.; Mani, S.G.;  Guggilapu, S. D.; Nagaraju, B.; Alarifi, A.; Kamal,A., Med. Chem. Comm., 2018, 9, 275.
  • Glycogen synthase kinase-3 and its inhibitors: potential target for various therapeutic conditions. Prashanth, S. A.; Harikrishna, N.; Hussaini, S.M.A.; Babu, B.N.; Kamal, A.,Eur. J. Med. Chem., 2018,144, 843.
  • Design, synthesis and biological evaluation of 1, 4-dihydroindeno[1,2-c]pyrazole linked oxindole analogues as potential anticancer agents targeting tubulin and inducing p53 dependent apoptosis. Irfan, A.; Rao G.K.; Makani, V.K.K.; Shareef, M. A.; Kumar, C.G.; Bhadra, M.P.; Kamal, A.,Eur. J. Med. Chem., 2018, 144, 104.
  • Synthesis of imidazo-thiadiazole linked indolinone conjugates and evaluated their microtubule network disrupting and apoptosis inducing ability. Narsimha, R.M.P.; Nagarju, B.; Jeshma, K.; Vishnuvardhan, M.V.P.S.; Pollepalli, S.; Jain, N.; Kamal, A.,  Bioorg. Chem., 2018, 76, 420.
  • Development of pyrrolo [2,1-c][1,4]benzodiazepineβ-glucosideprodrugs for selective therapy of cancer. Praveen, R.A.; Sayeed, I. B.; Shareef, M. A.; Nagarju, B.; Nagarajan, A.; Kamal, A., Bioorg. Chem., 2018, 76, 288.
  • Design, synthesis and biological evaluation of new β-carboline-bisindole compounds as DNA binding, photocleavage agents and topoisomerase I inhibitors. Jeshma, K.; Nagarju, B.; Nayak, V.L.; Ravikumar, A.; Rao, M.P.N.; Nagesh, N.; Kamal, A., Eur. J. Med. Chem., 2018, 143, 1563.
  • Synthesis of benzo[d]imidazo[2,1-b]thiazole-chalcone conjugates as microtubule targeting and apoptosis inducing agents. Sultana, F.; Bonam, S.R.; Reddy, V.G.; Nayak, V.L.; Ravikumar, A.; Routhu, S.R.; Alarifi, A.; Kamal, A., Bioorg. Chem., 2018, 76, 1.
  • Catalyst-free synthesis of pyrazole-aniline linked coumarin derivatives and their antimicrobial evaluation.Jeshma, K.; Nagaraju, B.;  Kumar, C.J.; Sirisha, K.; Chandrasekhar, Ch.; Alarifi, A.; Kamal, A.; J. Saudi Chem. Soc., 2018, 22, 665.
  • An efficient RuCl3·H2O/I2 catalytic system: A facile access to 3-aroylimidazo[1,2-a]pyridines from 2-aminopyridines and chalcones; Ramya, P. V. S.; Angapelly, S.; Digwal, C. S.; Yadav, U.; Babu, B. N.; Kamal, A., J. Saudi Chem. Soc., 2018, 22, 90.
  • Discovery of curcumin inspired sulfonamide derivatives as a new class of carbonic anhydrase isoforms I, II, IX, and XII inhibitors. Ramya, P.V.S.; Angapelly, S.; Angeli, A.; Digwal, C.S.;Arifuddin, Md.,Babu, B.N.; Supuran, C. T.; Kamal, A.,  J. Enzyme Inhbn. & Med. Chem., 2017, 32, 1274.
  • Lipases in asymmetric transformations: Recent advances in classical kinetic resolution and lipase-metal combinations for dynamic processes. Seddigi, Z.S.; Malik, M.S.; Ahmed, S. A; Babalghith, A.O.; Kamal, A., Coord.Chem.Rev., 2017, 348, 54.
  • Statistical optimization of production conditions of β-glucosidase from Bacillus stratosphericus strain SG9. Dutta, S.G.; Shaik, A.B.; Kumar, C.G.; Kamal, A.; 3 Biotech., 2017,7, 221.
  • Ultrasound assisted, VOSO4 catalyzed synthesis of 4-thiazolidinones: Antimicrobial evalution of indazole-4-thiazolidinone derivatives. Angapelly, S.; Ramya, P.V.S.; Rani, R.S.;  Kumar, C.G.; Kamal, A.; Arifuddin, Md., Tetrahedron, 2017, 58, 4632.
  • Design, synthesis and biological evaluation of noval pyrazolochalcones as potential modulators of PI3K/Akt/mTOR pathway and inducers of apoptosis in breast cancer cells. Shaik, A.B.; Rao, G.K.; Kumar, G.B.; Patel, N.; Reddy, V.S.; Khan, I.;  Kumar, C.G.; Veena, I.; Shekar, K.C.; Barkume, M.,  Jadhav, S.; Juvekar, A.; Kode, J.; Bhadra, M.P.; Kamal, A., Eur. J. Med. Chem., 2017, 139, 305.
  • A facile one-pot CC and CN bond formation for the synthesis of spiro-benzodiazepines and their cytotoxicity.  Nagarju, B.; Jeshma, K.; Nayak, V.L.; Praveen, R.A.; Alarifi, A.; Kamal, A., Tetrahedron, 2017, 73, 6969.
  • Synthesis of substituted phenanthrene-9-benzimidazole conjugates: Cytotoxicity evaluation and apoptosis inducing studies.  Kumar, N.P.; Sharma, P.; Kumari, S.S.; Brahma,U.; Nekkati, S.; Shankariah, N.; Kamal, A., Eur. J. Med. Chem., 2017, 140, 128.
  • Molecular iodine-promoted transimination for the synthesis of 6-phenylpyrido[2′,1′:2,3]imidazo[4,5-c]quinoline and 6-(pyridin-2-yl)pyrido[2′,1′:2,3]imidazo[4,5-c]quinolones. Satish.S.; Shaik P.S.; Rao, A.V.S.; Harikrishna, N.; Alarif, A.; Kamal, A., Asian J. Org. Chem., 2017, 6, 1830.
  • Telomerase inhibition and human telomeric G‑quadruplex DNA stabilization by a β‑Carboline-benzimidazole derivative at low concentrations. Yadav, K.; Meka, P.N.R.; Guggilapu, S.S.S.D.;Jeshma, K.; Kamal, A.; Srinivas, R.; Devayani, P.; Babu, B.N.; Nagesh, N.; ACS Biochemistry, 2017, 56, 4392.
  • Design, synthesis and biological evaluation of 2-anilinopyridyl-linked oxindole conjugates as potent tubulin polymerisation inhibitors. Sultana, F.; Shaik, P.S.; Nayak, V. L.; Hussaini, S.M.A.; Marumudi, K; Shaik, T.B.; Sridevi. B.; Alarifi, A.; Kamal, A., Chemistry Select, 2017, 2, 9901.
  • Recent advances in combretastatins based derivatives and prodrugs as antimitotic agents. Seddigi, Z.S.; Malik, M.S.; Prashanth, S.A.; Ahmed, S.; Babalghith, A.O.; Lamfon, H.A.; Kamal, A., Med. Chem. Commun., 2017, 8, 1592.
  • Annulation of 4-hydroxypyrones and α-keto vinyl azides; A regiospecific approach towards the synthesis of furo[3, 2-c]pyrone scaffolds under catalyst free condition. Prasad, B.; Reddy,V.G.; Harikrishna N.; Subba Reddy, N.V.; Alarifi. A.; Kamal, A., Chemistry Select, 2017, 2, 8122.
  • Visible light driven coupling of 2-aminopyridines and α-keto vinyl azides for the synthesis of imidazo[1, 2-a]pyridines and their cytotoxicity. Praveen R.A.; Sastry, K.N.V; Jeshma K; Reddy V.G.; Nagarajan, A.; Sayeed, I.B.; Kamal, A., Chemistry Select, 2017, 2, 8158.
  • An efficient one-pot approach for the regio and diastereoselective synthesis of trans-dihydrofuran derivatives: cytotoxicity and DNA-binding studies. Tangella, Y.; Manasa, K.L.; Sathish, M.; Nayak, V.L.; Alarifi. A.; Nagesh, A.; Kamal, A., Org. Biomol. Chem., 2017, 15, 6837.
  • Development and biological evaluation of imidazothiazole propenones as tubulin inhibitors that effectively triggered apoptotic cell death in alveolar lung cancer cell line. Sayeed, I.B.; Rao, G.K.; Makani, V.K.K; Nagarajan, A; Shareef, M.A.; Alarifi, A.; Bhadra, M.P.; Kamal, A., Chemistry Select, 2017, 2, 6480.
  • A facile I2-catalyzed synthesis of imidazo[1,2-a]pyridines via sp3 C-H functionalization of azaarenes and evaluation of anticancer activity. Geeta, S.M.;Shaik, P.S.; Tangella, Y.; Bale, S.; Godugu, C.; Kamal, A., Org. Biomol. Chem., 2017, 15, 6780.
  • Vanadium-catalyzed oxidative C(CO)C(CO) bond cleavage for CN bond formation: One-pot domino transformation of 1,2-diketones and amidines into imides and amides. Digwal, C.S.; Yadav, U.; Ramya, P.V.S.; Sana, S.; Swain, B.; Kamal, A., J. Org. Chem., 2017, 82, 7332.
  • Click chemistry-assisted synthesis of triazolo linked podophyllotoxin conjugates as tubulin polymerization inhibitors. Vishnuvardhan, M.V.P.S.; Saidireddy, V.; Chandrashekar, V.; Nayak, V.L; Sayeed, I.B; Alarifi, A; Kamal, A., Med.Chem.Commun., 2017, 8, 1817.
  • Synthesis and biological evaluation of chalcone-linked pyrazolo[1,5-a]pyrimidines as potential anticancer agents. Bagul, C; Rao, G.K.; Makani, K.K.V.; Tamboli, J.R.; Bhadra, M.P.; Kamal, A., Med.Chem.Commun., 2017, 8, 1810.
  • Copper-catalysed tandem synthesis of substituted quinazolines from phenacyl azides and o-carbonyl anilines. Sastry, K.N.V.; Prasad, B.; Nagaraju, B.; Reddy, V.G.; Alarifi, A.; Babu, B. N.; Kamal, A., Chemistry Select, 2017, 2, 5378.
  • New quinoline linkedchalcone and pyrazoline conjugates: Molecular properties prediction, antimicrobial and antitubercular activities. Rao, N.S.; Shaik, A.B.; Routhu, S.R.; Hussaini,S.M.A.;Sunkari, S.; Rao, A.V.S.; Reddy, A.M.; Alarifi, A.; Kamal, A.,Chemistry Select, 2017, 2, 2989.
  • Transition-metal-free oxidative cross-coupling of methylhetarenes with imidazoheterocycles towards efficient C(sp2)−H carbonylation. Sultana, F.; Shaik, S.P.; Alarifi, A.; Srivastava, A.K.; Kamal, A., Asian J. Org. Chem., 2017, 6, 890.
  • Diphenylphosphoryl azide (DPPA)-mediated one-pot synthesis of oxazolo[4,5-c][1,8]naphthyridin-4(5 H)-ones,oxazolo[4,5-c] quinolone-4(5 H)-ones, and tosyloxazol-5-yl pyridines. Tangella, Y.; Manasa, K. L.; Sathish, M.; Alarifi, A.; Kamal, A.,Asian J. Org. Chem., 2017, 6, 898.
  • Metal-free C‒C bond cleavage: One-pot access to 1,4-benzoquinone linked N-formyl amides/sulfonamides/carbamates using oxone. Ramya, P.V.S.; Angapelly, S.; Babu, B.N.; Digwal, C.S.; Nagarsenkar, A.; Srinivasulu, G.; Prasanth, B.; Arifuddin, Md.; Kanneboina, K.; Rangan, K.; Kamal, A.,Asian J. Org. Chem., 2017, 6, 1008.
  • One pot synthesis of naphtho [1',2':4,5] imidazo[1,2-a]pyridin-5-yl(aryl)methanones via a sequential Sonogashira coupling/alkyne-carbonyl metathesis.  Baig, M.F.; Shaik, P.S.; Krishna, H.N.; Chouhan, K.N.; Alarifi, A.; Kamal, A., Eur. J. Org. Chem., 2017, 4026.
  • Design, synthesis, and in vitro and in-vivo evaluations of (Z)-3,4,5-trimethoxystyrylbenzenesulfonamides/sulfonates as highly potent tubulin polymerization inhibitors. Mahesh, R; Nayak, V.L; Babu, K.S.; Riyaz, S.; Shaik, T.B.; Kumar, G.B.; Mallipeddi, P.L.; Reddy, C.R.; Shekar, K.C.; Jose, J.; Nagesh, N.; Kamal, A., ChemMedChem., 2017, 12, 678.
  • Rational design and synthesis of 2-anilinopyridinylbenzothiazole    schiff bases as antimitotic agents. Thoukhir, B.S.; Hussaini, S.M.A.; Nayak, V.L.; Sucharitha M.L.; Malik, M.S.; Kamal, A., Bioorg. Med. Chem. Lett., 2017, 27, 2549.
  • Design and synthesis of 1,2,3-triazolo linked benzo[d]imidazo[2,1-b]thiazole conjugates as tubulin polymerization inhibitors. Shaik, P.S.; Vishnuvardhan, M.V.P.S.; Sultana, F.; Rao, A.V.S.; Bagul, C.; Bhattacharjee, D.; Kapure, J.S; Jain, N.; Kamal, A., Bioorg. Med. Chem., 2017, 25, 3285.
  • Sulfamic acid catalyzed one-pot, three-component green approach: synthesis and cytotoxic evaluation of pyrazolyl-thiazole congeners. Meshram, H.M.; Sridevi, B.; Tangella, Y.; Korrapati, S.B.; Nanubolu, J.B.; Routhu, S.R.; Kumar C.G.; Kamal, A., New J. Chem., 2017,41, 3745. 
  • Phenacyl azides as efficient intermediates: one-pot synthesis of pyrrolidines and imidazoles. Reddy, N.C.; Sathish, M.; Adhikary, S.; Nanubolu, J.B.; Alarifi, A.; Maurya, R.A.; Kamal, A., Org. Biomol. Chem. 2017, 15, 2730.
  • Design, synthesis and biological evaluation of imidazopyridine-propenone conjugates as potent tubulin inhibitors. Sayeed, I.B.; Nayak, V.L.; Shareef, M.A.; Chouhan, N.K.; Kamal, A., Med.Chem.Comm., 2017, 8, 1000.
  • 2-Arylaminobenzothiazole-arylpropenone conjugates as tubulin polymerization inhibitors.  Rao, A.V.S.; Rao, B.B.; Sunkari, S.; Shaik, P.S.; Shaik, B.; Kamal, A., Med.Chem.Comm. 2017, 8, 924.
  • Synthesis and biological evaluation of curcumin inspired indole analogues as tubulin polymerization inhibitors.Ramya, P.V.S.; Angapelly, S.; Guntuku, L.; Digwal, C.S.; Babu, B.N.; Naidu, V.G.M.; Kamal, A., Eur. J. Med. Chem., 2017, 127, 100.
  • 2-aryl benzimidazole conjugate induced apoptosis in human breast cancer MCF-7 cells through caspase independent pathway. Nayak, V.L; Nagesh, N.; Ravikumar, A; Bagul, C.; Vishnuvardhan, M.V.P.S.; Srinivasulu, V; Kamal, A., Apoptosis, 2017, 22, 118.
  • Synthesis and biological evaluation of cis-restricted triazole/tetrazole mimics of combretastatin-benzothiazole hybrids as tubulin polymerization inhibitors and apoptosis inducers.Rao, A.V.S; Swapna, K; Shaik, P.S; Nayak, V.L; Reddy, T.S; Sunkari, S; Shaik, T.S; Bagul, C; Kamal, A., Bioorg. Med. Chem., 2017, 25, 977.
  • Synthesis of 2,3,6,7-tetramethoxyphenanthren-9-amine: An efficient precursor to access new 4-aza-2,3-dihydropyrido phenanthrenes as apoptosis inducing agents. Kumar, N.P;  Sharma, T.P; Reddy, S; Nekkanti, S; Shankaraiah, N; Lalita, G; Sujanakumari, S; Bhargava, S.K; Naidu, V.G.M; Kamal, A., Eur. J. Med. Chem., 2017, 127, 305.
  • Metal‐free aerobic oxidative C−C bond cleavage between the carbonyl carbon and the α‐carbon of α‐azido ketones: anovel synthesis of N‐alkylated benzamides. Reddy, C.N; Krishna, N.H; Reddy, V.G; Alarifi, A; Kamal, A., Asian J. Org. Chem., 2017, 6, 1498.
  • Iodine-catalyzed Csp3-H functionalization of methylhetarenes: One-pot synthesis and cytotoxic evaluation of heteroarenyl-benzimidazoles and benzothiazole. Baig, M.F; Shaik, S.P; Nayak, V.L; Alarifi, A; Kamal, A., Bioorg. Med. Chem., 2017, 27, 4039.
  • Regioselective oxidative cross-coupling of benzo[d]imidazo[2,1-b]thiazoles with styrenes: a novel route to C3-dicarbonylation. Shaik, S.P; Sultana, F; Ravikumar, A; Sunkari, S; Alarifi, A; Kamal, A., Org. Biomol. Chem., 2017, 15, 7696.
  • Design and synthesis of imidazo[2,1-b]thiazole linked triazole conjugates: Microtubule-destabilizing agents. Shaik, P.S; Nayak, V.L;  Sultana, F; Rao, A.V.S; Shaik, A.B; Babu, K.S; Kamal, A., Eur. J. Med. Chem., 2017, 126, 36.
  • Synthesis of novel C3-linked β-carboline-pyridine derivatives employing khronke reaction: DNA-binding ability and molecular modeling studies. Shankaraiah, N.; Sharma, P.; Pedapati, S.; Nekkanti, S.; Srinivasulu, V.; Kumar, N. P.; Kamal, A. Lett. in Drug Design & Discovery, 2016, 13, 335.
  • Synthesis and biological evaluation of imidazopyridinyl-1,3,4-oxadiazole conjugates as apoptosis inducers and topoisomerase IIa inhibitors. Rao, A.V.S; Vishnuvardhan, M.V.P.S.; Reddy, N.V.S; Reddy, T.S; Shaik, P.S; Bagul, C; Kamal, A., Bioorg. Chem., 2016, 69, 7.
  • VOSO4 catalyzed highly efficient synthesis of benzimidazoles, benzothiazoles, and quinoxalines. Digwal, C.S.; Yadav, U; Sakla, A.P; Ramya, P.V.S; Aaghaz, S; Kamal, A., Tet. Lett., 2016, 57, 4012
  • An efficient synthesis of 2-substituted benzimidazoles via photocatalytic condensation of o-phenylenediamines and aldehydes. Jeshma, K; Nagaraju, B; Kamal, A; Srivastava, A.K., ACS Comb. Sci., 2016, 18, 644.
  • Design, synthesis and biological evaluation of N-((1-benzyl-1H-1,2,3-triazol-4-yl)methyl)-1,3-diphenyl-1H-pyrazole-4-carboxamides as CDK1/Cdc2 inhibitors.Reddy, V.G; Reddy, T.S; Nayak, V.L; Prasad, B; Reddy, A.P; Ravikumar, A; Taj, S; Kamal, A., Eur. J. Med. Chem. 2016, 122,164.
  • Phenyliodonium diacetate mediated one-pot synthesis of benzimidazoles and quinazolinones from benzylamines. Yellaiah, T; Manasa, K.L; Sathish, M; Alarifi, A; Kamal, A., Chemistry Select, 2016, 1, 2895.
  • Design and synthesis of cis-restricted benzimidazole and benzothiazole mimics of combretastatin A-4 as antimitotic agents with apoptosis inducing ability. Ashraf,Md.; Thokhir, B.S; Malik, M.S; Syed, R; Mallipeddi, P.L; Vishnuvardhan,M.V.P.S; Kamal, A., Bioorg. Med. Chem. Lett., 2016, 26, 4527.
  • Investigation of the apoptotic pathway induced by benzimidazole–oxindole conjugates against human breast cancer cells MCF-7. Nayak, V.L; Nagaseshadri, B; Vishnuvardhan, M.V.P.S; Kamal, A; Bioorg. Med. Chem. Lett., 2016, 26, 3313.
  • Synthesis and biological evaluation of arylcinnamide linked combretastatin-A4 hybrids as tubulin polymerization inhibitors and apoptosis inducing agents.Kamal, A; Bajee, S; Nayak, V.L; Rao, A.V.S; Nagaraju, B; Reddy, Ch.R; Kapure J.S; Alarifi, A., Bioorg. Med. Chem. Lett., 2016, 26, 2957.
  • Synthesis, DNA binding affinity and anticancer activity of novel 4H-benzo[g][1,2,3]triazolo[5,1-c][1,4]oxazocines. Sastry, K.N.V; Routhu, S.R; Gupta, S; Nagesh, N; Babu, N.B; Kumar, C.G; Maurya, R.A; Kamal, A., Org. Biomol. Chem., 2016, 14, 9294.
  • 2-Anilino-3-Aroylquinolines as potent tubulin polymerization inhibitors. Srikanth, P.S; Nayak, V.L; Babu, K.S; Kumar, G.B; Ravikumar, A; Kamal, A., ChemMedChem., 2016, 11, 2050.
  • Benzo[b]furan derivatives induces apoptosis by targeting the PI3K/Akt/mTOR signaling pathway in human breast cancer cells. Kamal, A; Nayak, V.L; Nagesh, N; Vishnuvardhan, M.V.P.S; Reddy, N.V.S., Bioorg. Chem., 2016, 66, 124.
  • Iron-mediated one-pot synthesis of 3, 5-diarylpyridines from β-nitrostyrenes. Satish, M; Chetna, J; Krishna, N.H; Shankaraiah, N; Alarifi, A; Kamal, A., J. Org. Chem., 2016, 81, 2159.
  • Access to imidazole derivatives by silver(I) carbonate mediated coupling of vinyl azides with secondary amines.  Adiyala, P.R; Borra, S; Kamal, A; Maurya, R.W., Eur. J. Org. Chem., 2016, 7, 1269.
  • Synthesis and biological evaluation of 1,2,3-triazole tethered pyrazoline and chalcone derivatives. Hussaini, S.M.A; Yedla, P; Babu, K.S; Shaik, T.B; Kumar, C.G; Kamal, A., Chem. Bio. & Drug. Design., 2016, 88, 97.
  • An evaluation of the CYP2D6 and CYP3A4 inhibition potential of metoprolol metabolites and their contribution to drug-drug and drug-herb interaction by LC-ESI/MS/MS. Borkar, R; Bhandi, M.M; Dubey, A.P; Reddy, V.G; Komirishetty, P; Nandekar, P.P;  Sangamwar, A.T; Kamal, A; Banerjee, S.K; Ragampeta, S., Biomed. Chromatography, 2016, 30, 1556.
  • TBAI/TBHP-catalyzed[3+2]cycloaddition/oxidation/aromatization cascade and online ESI-MS mechanistic studies: synthesis of pyrrolo[2,1-a]isoquinolines and indolizino[8,7-b]indoles. Nekkanti, S; Kumar, N.P; Sharma, P; Kamal, A; Nachtigall, F.M; Doria, O.F; Santos, L.S; Shankaraiah, N., RSC Adv. 2016, 6, 2671.
  • Design, synthesis and antiproliferative activity of the new conjugates of E7010 and resveratrol as tubulin polymerization inhibitors. Kamal, A; Ashraf, Md.; Shaik, T.B; Hussaini, S.M.A; Singh, S; Vishunvardha, M.V.P.S; Kiran, B; Sridhar, B., Org. Biomol. Chem., 2016, 14, 1382.
  • Silver catalyzed domino aza-annulation/diels–Alder cyclization of 2-ene-yne anilines: A facile one-pot access to carbazole, dihydrocarbazole and tetrahydrocarbazole frameworks. Krishna, H.N; Saraswati, A.P; Sathish, M; Shankaraiah, N; Kamal, A., Chem. Commun., 2016, 52, 4581.
  • A novel quinazolinone chalcone derivative induces mitochondrial dependent apoptosis and inhibits PI3K/Akt/mTOR signaling pathway in human colon cancer HCT-116 cells. Wani, Z.A; Guru, S.K; Rao, A.V.S; Sharma, S; Mahaja, G; Behl, A; Kumar, A; Sharma, P.R; Kamal, A; Bhushan, S; Mondhe, D.M., Food  Chem. Toxicol., 2016, 87, 1.
  • Discovery of pyrrolospirooxindole derivatives as novel cyclin dependent kinase-4 (CDK4) inhibitors by catalyst-free, green approach. Kamal, A; Mahesh, R; Nayak, V.L;  Babu, K.S; Kumar, G.B; Shaik, A.B; Kapure, J.S; Alarifi, A., Eur. J. Med. Chem., 2016, 108, 476.
  • Design and synthesis of C3-tethered 1,2,3-triazolo-β-carboline derivatives: anticancer activity, DNA-binding ability, viscosity and molecular modeling studies. Shankaraiah, N; Jadala, C; Nekkanti, S; Senwar, K.R; Nagesh, N; Shrivastava, S; Naidu, V.G.M; Sathish, M; Kamal, A., Bioorg. Chem., 2016, 64, 42.
  • The molecular structure of thio-ether fatty acids influences PPAR-dependent regulation of lipid metabolism. Lund, J; Stensrud, C; Rajender, Bohov, P; Thoresen, G.H; Berge, R.K; Wright, M; Kamal, A; Rustan, A.C; Miller, A.D; Skorve, J; Bioorg. Med. Chem., 2016, 24, 1191.
  • Synthesis of (Z)-1-(1,3-diphenyl-1H-pyrazol-4-yl)-3-(phenylamino) prop-2-en-1-one derivatives as potential anticancer and apoptosis inducing agents. Reddy, T.S; Reddy, V.G; Kulhari, H; Shukla, R; Kamal, A; Bansal, V., Eur. J. Med. Chem., 2016, 117, 157.
  • Combretastatin linked 1,3,4-oxadiazole conjugates as a potent tubulin polymerization inhibitors. Kamal, A; Srikanth, P.S; Vishnuvardhan, M.V.P.S; Kumar, G.B; Babu, K.S; Hussaini, S.M.A; Kapure, J.S; Alarifi, A., Bioorg. Chem., 2016, 65, 126.
  • Synthesis and mechanistic aspects of 2-anilinonicotinyl-pyrazolo[1,5-a]pyrimidine conjugates that regulate cell proliferation in MCF-7 cells via estrogen signalling. Kamal, A; Faazil, S; Hussaini, S.M; Ramaiah, M.J; Balakrishna, M; Patel, N; Pushpavalli, S.N.C.V.L; Bhadra, M.P., Bioorg. Med. Chem. Lett., 2016, 26, 2077.
  • Copper-catalyzed three-component synthesis of aminon-aphthoquinone–sulfonylamidine conjugates and in vitro evaluation of their antiproliferative activity. Suja, T.D; Divya, K.V.L; Nayak, V.L; Ravikumar, A; Kamal, A., Bioorg. Med. Chem. Lett., 2016, 26, 2072.
  • Design, synthesis of phenstatin/isocombretastatin-oxindole conjugates as antimitotic agents. Kumar, G.B; Nayak, V.L; Sayeed, I.B; Reddy, V.S; Shaik, A.B; Mahesh, R; Baig, M.F; Shareef, M.A; Ravikumar, A; Kamal, A., Bioorg. Med. Chem. 2016, 24, 1729.
  • Convenient synthesis of substituted pyrroles via cerium (IV) ammonium nitrate (CAN)-catalyzed paal-knorr reaction. Kamal, A.; Faazil, S.; Malik, M. S.; Balakrishna, M.; Bajee, S.; Siddiqui, M.R.H.; Alarifi, A., Arabian Journal of Chemistry, 2016, 9, 542.
  • Novel podophyllotoxin-thiourea congeners as DNA topoisomerase-II inhibition and apoptosis inducing agents: Synthesis, anticancer activity and molecular modeling studies; Shankaraiah, N.; Kumar, N. P.; Amula, S. B.; Nekkanti, S.; Jeengar, M. K.; Naidu, V. G. M.; Reddy, T. S.; Kamal, A., Bioorg. Med. Chem. Lett. 2015, 25, 4239. 
  • Chemical preservatives-based storage studies and ethanol production from juice of sweet sorghum cultivar, ICSV 93046. Kumar, C.G; Rao, P.S; Gupta, S; Malapaka, J; Kamal, A., Sugar Tech, 2015, 17, 404.
  • Isolation and characterization of cellulose from sweet sorghum bagasse. Kumar, C.G; Kumar, M.P; Gupta, S; Sunder, M.S; Rao, K.V.M; Jagadeesh, B; Swapna, V; Kamal, A., Sugar Tech, 2015, 17, 395.
  • Synthesis of (Z)-(arylamino)-pyrazolyl/isoxazolyl-2-propenones as tubulin targeting anticancer agents and apoptotic inducers.  Kamal, A; Reddy, V.S; Shaik, A.B; Kumar, G.B; Vishnuvardhan, M.V.P.S; Polepalli, S; Jain, N., Org. Biomol. Chem., 2015, 13, 3416.
  • Synthesis of phenstatin/isocombretastatin–chalcone conjugates as potent tubulin polymerization inhibitors and mitochondrial apoptotic inducers. Kama, A; Kumar, G.B; Vishnuvardhan, M.V.P.S; Shaik, A.B; Reddy, V.S; Mahesh, R; Sayeeda, I.B; Kapure, J.S., Org. Biomol. Chem., 2015, 13, 3963.
  • An efficient one-pot decarboxylative aromatization of tetrahydro-β-carbolines by using N-chlorosuccinimide: total synthesis of norharmane, harmane and eudistomins. Kamal, A; Sathish, M; Prasanthi, A.V.G; Chetna, J; Tangella, Y; Srinivasulu, V; Shankaraiah, N; Alarifi, A; RSC Adv. 2015, 5, 90121.
  • Synthesis of 2-anilinopyridine–arylpropenone conjugates as tubulin inhibitors and apoptotic inducers. Kamal, A; Reddy, V.S; Vishnuvardha, M.V.P.S; Kumar, G.B; Shaik, A.B;  Chourasiya, S.S; Reddy, M.K; Sayeed, I.B; Adiyala, P.R; Jain, N; RSC Adv. 2015, 5, 97367.
  • Novel etoposide analogue modulates expression of angiogenesis associated microRNAs and regulates cell proliferation by targeting STAT3 in breast cancer. Srinivas, C.M; Ramaiah, J; Lavanya, A; Suresh, Y; Kishor, P.B.K; Shaik, A.B; Kamal, A; Bhadra, U; Bhadra, M; Plos One, 2015, DOI:10.1371/ journal.pone.0142006.
  • Amberlite IR-120H: An ef?cient and recyclable heterogeneous catalyst for the synthesis of pyrrolo[1,2-a]quinoxalines and 5'H-spiro[indoline-3,4'-pyrrolo[1,2a]quinoxalin]-2-ones. Kamal, A; Babu, K.S; Kovvuri, J; Manasa, V; Ravikumar, A; Alarifi; Tetrahedron Lett., 2015, 56, 7012.
  • Synthesis and biological evaluation of benzimidazole-oxindole conjugates as microtubule-targeting agents. Kamal, A; Nagaseshadri, B; Nayak, V.L; Srinivasulu, V; Sathish, M; Kapure, J.S; Reddy, C.S., Bioorg. Chem., 2015, 63, 72.
  • Design and synthesis of dithiocarbamate linked β-carboline derivatives: DNA topoisomerase II inhibition with DNA binding and apoptosis inducing ability.  Kamal, A; Sathish, M; Nayak, V.L; Srinivasulu, V; Kavitha, B; Tangella, Y;  Thummuri, D; Bagul, C; Shankaraiah, N; Nagesh, N.,  Bioorg. Med. Chem. 2015, 23, 5511.
  • Aryl-imidazothiadiazole analogues as microtubule disrupting agents. Kamal, A; Rao, A.V.S; Reddy, T.S; Polepalli, S; Shaik, P.S; Bagul, C; Vishnuvardhan, M.V.P.S; Jain, N., Med.Chem.Comm. 2015, 6, 1842.
  • Catalyst-free, one pot and three-component synthesis of 4'-phenyl-1'H-spiro[indoline-3,2'-quinazolin]-2-ones. Kamal, A; Babu, K.S; Chandrasekhar, C; Sastry, K.N.V; Nagaraju, B; Kumar, C.G., Tetrahedron Lett., 2015, 56, 6373.
  • Investigation of the mechanism and apoptotic pathway induced by 4β cinnamido linked podophyllotoxins against human lung cancer cells A549. Kamal, A; Nayak, V.L; Bagul, C; Mallareddy, A; Vishnuvardhan, M.V.P.S., Apoptosis, 2015, 20, 1518.
  • Design and synthesis of pyrazole/isoxazole linkedarylcinnamides as tubulin polymerizationinhibitors and potential antiproliferative agents. Kamal, A; Shaik, S.B; Rao, B.B; Khan, I; Kumar, G.B; Jain, N., Org. Biomol. Chem., 2015, 13, 10162.
  • H2O-mediated isatin spiro-epoxide ring opening with NaCN: synthesisof novel 3-tetrazolylmethyl-3-hydroxy-oxindole hybrids and theiranticancer evaluation. Sharma, P; Senwar, K.R; Jeengar, M.K; Reddy, T.S; Naidu, V.G.M: Kamal, A; Shankaraiah, N; Eur. J. Med. Chem., 2015, 104, 11.
  • Spirooxindole-derived morpholine-fused-1, 2, 3 - triazoles: Design, synthesis, cytotoxicity and apoptosis inducing studies.  Senwar, K.R; Sharma, P; Reddy, T.S; Jeengar, M.K; Nayak, V.L; Naidu, V.G.M.; Kamal, A; Shankaraiah, N., Eur. J. Med. Chem. 2015, 102, 413.
  • Synthesis and biological evaluation of pyrazole-triazole hybrids as cytotoxic and apoptosis inducing agents. Reddy, T.S; Kulhari, H; Reddy, V.G; Rao, A.V.S; Bansal, V; Kamal, A; Shukla, R.,               Org. Biomol. Chem., 2015, 13, 10136.
  • Synthesis and biological evaluation of spiro[cyclopropane-1,3-indolin]-2-ones as potential anticancer agents. Reddy, C.N; Nayak, V.L; Mani, G.S.; Kapure, J.S; Adiyala, P.R; Maurya, R.W; Kamal, A., Bioorg. Med. Chem. Lett., 2015, 25, 4580.
  • One-pot synthesis of podophyllotoxin-thiourea congeners by employing NH2SO3H/Nal: Anticancer activity, DNA topoisomerase-II inhibition, and apoptosis inducing agents.  Shankaraiah, N; Kumar, N.P; Amula, S.B; Nekkanti, S;Jeengar, M.K; Naidu, V.G.M; Reddy, T.S; Kamal, A., Bioorg. Med. Chem. Lett., 2015, 25, 4239.
  • Biological activities of pyrenyl-derived thiosemicarbazone half-sandwich complexes. Raja, N; Devika, N; Gupta, G; Nayak, V.L; Kamal, A; Nagesh, N; Therrien, B., Journal of Organometallic Chemistry, 2015, 794, 104.
  • Synthesis and antimicrobial potential of nitrofuran-triazole congeners. Kamal, A; Hussaini, S.M.A; Sucharitha M.L; Chandra, P; Sultana, F; Kumar, C.G., Org. Biomol. Chem., 2015, 13, 9388.
  • Bisindole-PBD regulates breast cancer cell proliferation via SIRT-p53 axis. Sarma, P; Bag, I; Ramaiah, J; Kamal, A; Bhadra, U; Bhadra, M.P., Cancer Biology & Therapy, 2015, 16, 1486.
  • Anticancer activity of a novel quinazolinone-chalcone derivative through cell cycle arrest in pancreatic cancer cell line. Wani, Z.A; Pathania, A.S; Mahajan, G; Behl, A; Mintoo, M.J; Guru, S.K; Viswanath, A; Malik, F.Z; Kamal, A; Mondhe, D.M., J. Solid Tumors, 2015, 5, 2.
  • Synthesis and biological evaluation of phaitanthrin congeners as anti-mycobacterial agents. Kamal, A; Reddy, B.V.S; Sridevi, B; Ravikumar, A; Venkateswarlu, A; Sravanthi, G; Sridevi, J.P; Yogeeswari, P; Sriram, D., Bioorg. Med. Chem. Lett. 2015, 25, 3867.
  • Design, synthesis and biological evaluation of 1,3-diphenyl-1H-pyrazole derivatives containing benzimidazole skeleton as potential anticancer and apoptosis inducing agents. Reddy, T.S.; Kulhari, H; Reddy, V.G; Bansal, V; Kamal, A; Shukla, R., Eur. J. Med. Chem. 2015, 101, 790.
  • Embracing synthetic lethality for novel anticancer therapies. Kamal, A; Shaik, T.B; Malik, M.S., Expert Opinion on Drug Discovery, 2015, 10, 1119.
  • Synthesis of 2-aryl-1,2,4-oxadiazolo-benzimidazoles: Tubulin polymerization inhibitors and apoptosis inducing agents. Kamal, A; Reddy, T.S.; Vishnuvardhan, M.V.P.S.; Nimbarte, V.K.; Rao, A.V.S.; Srinivasulu, V.; Shankaraiah, N., Bioorg. Med. Chem. 2015, 23, 4608.
  • Synthesis and biological evaluation of benzo[d][1,3]dioxol-5-yl chalcones as anti-proliferating agents.Balakrishna, M; Reddy, V.L; Riyaz, Sd.; Bagul,C.; Satyanarayana, B.M.; Rao, J.V., Chem. Biol. Drug Des., 2015,  86, 1267
  • Sulfamic acid: An efficient and recyclable solid acid catalyst for the synthesis of 4, 5-dihydropyrrolo[1,2-a]quinoxalines. Kamal, A; Babu, K.S.; Hussaini, S.M.A.; Srikanth, P.S.; Balakrishna, M; Alarifi, A., Tetrahedron Lett., 2015, 56, 4619.
  • Cu(OAc)2/Et3N mediated oxidative coupling of α-azido ketones with pyridinium ylides: Utilizing in situ generated imines for regioselective synthesis of imidazo[1,2-a]pyridines, Kamal, A; Reddy, C.N.; Satyaveni, M.; Chandrasekhar, D.; Nanubolu,J.B.; Singarapu, K.K.; Maurya, R.M., Chem. Commun., 2015, 51, 10475.
  • PhI(OAc)2-mediated one-pot oxidative decarboxylation and aromatization of tetrahydro-β-carbolines: synthesis of norharmane, harmane, eudistomin U and eudistomin I. Kamal, A.; Tangella, Y.;  Manasa, K.L.; Sathish, M.; Srinivasulu, V.; Chetna, J.; Alarifi, A., Org. Biomol. Chem., 2015, 13, 8652.
  • Podophyllotoxin derivatives: a patent review (2012-14). Kamal, A; Hussain, S.M.A.; Rahim, A.; Riyaz, Sd., Expert Opinion on Therapeutic Patents. 2015, 25, 1025.
  • A one-pot ‘click’ reaction from spiro-epoxides catalyzed by Cu(I)-pyrrolidinyl-oxazole-carboxamide. Senwar, K.R.; Sharma, P.; Nekkanti, S.; Sathish, M.; Kamal, A.; Sridhar, B.; Shankaraiah, N., New J. Chem., 2015, 39, 3973.
  • One-pot, three-component approach to the synthesis of 3,4,5-trisubstituted pyrazoles.  Kamal, A.; Sastry, K.N.; Chandrasekhar, D.; Mani, G.S.; Adiyala, P.R.; Nanubolu, J.B.; Maurya, R.A.; J. Org Chem. 2015,  9, 4325.
  • Amberlite IR-120H, an efficient and recyclable solid phase catalystfor the synthesis of quinoxalines: a greener approach.  Kamal, A.; Babu, K.S.; Hussaini, S.M.A.; Mahesh, R.; Alarifi, A., Tetrahedron Lett., 2015, 56, 2803.
  • Sulfamic acid promoted one-pot three-component synthesis and cytotoxic evaluation of spirooxindoles. Kamal, A.; Babu, K.S.; Vishnuvardhan, M.V.P.S.; Hussaini, S.M.A.; Mahesh, R.; Shaik, S.P.; Alarifi, A., Bioorg. Med. Chem. Lett., 2015, 25, 2199.
  • Synthesis of 2-anilinopyridyl-triazole conjugates as antimitotic agents. Kamal, A.; Rao, A.V.S.; Vishnuvardhan, M.V.P.S.; Reddy, T.S.; Swapna, K.; Bagul, C.; Reddy, N.V.S.; Srinivasulu, V., Org. Biomol. Chem., 2015, 13, 4879.
  • DNA-binding affinity and anticancer activity of b-carboline-chalcone conjugates as potential DNA intercalators: molecular modelling and synthesis. Shankaraiah, N.; Siraj, K.P.; Nekkanti, S.; Srinivasulu, V.; Sharma, P.; Senwar, K.R.S.; Satish, M.; Vishnuvardhan, M.V.P.S.; Ramakrishna, S.; Jadala, C.; Nagesh, N.; Kamal, A., Bioorg. Chem., 2015, 59, 130.
  • Design, synthesis and biological evaluation of imidazopyridine/imidazopyrimidine-benzimidazole conjugates as potential anticancer agents. Kamal, A.; Kumar, G.B.; Nayak, V.L.; Reddy, V.S.; Shaik, A.B.; Rajender, Reddy, M.K., Med.Chem.Comm., 2015, 6, 606.
  • Design and synthesis of pyrazole-oxindole conjugates targeting tubulin polymerization as new anticancer agents. Kamal A.; Shaik A.B.; Jain N.; Kishor C.; Nagabhushana A.; Supriya B.; Kumar G.B.; Chourasiya S.S.; Suresh Y.; Mishra R.K.; Addlagatta A., Eur. J. Med. Chem., 2015, 92, 501.
  • Synthesis of arylpyrazole linked benzimidazole conjugates as potential microtubule disruptors. Kamal, A.; Shaik, A.B.;Sowjanya, P.;Kumar, G.B.; Reddy, V.S.;Mahesh, R.; Garimella, S.; Jain, N., Bioorg. Med. Chem., 2015, 23, 1082.
  • Synthesis of phenstatin/isocombretastatin-chalcone conjugates as potent tubulin polymerization inhibitors and mitochondrial apoptotic inducers.  Kamal, A.; Kumar, G.B.; Vishnuvardhan, M.V.P.S.; Shaik, A.B.; Reddy, V.S.; Mahesh, R.; Sayeeda, I.B.; Kapure, J.S., Org. Biomol. Chem., 2015, 13, 3963.
  • Therapeutic potential of benzothiazoles:  a patent review (2010-2014).  Kamal, A.; Hussaini, S.M.A.; Malik, M.S., Expert Opinion on Therapeutic Patents 2015, 25, 335.
  • Regioselective synthesis, antimicrobial evaluation and theoretical studies of 2-styryl quinolones. Kamal, A.; Rahim, A.; Riyaz, Sd.; Poornachandra, Y.; Balakrishna, M.; Kumar, C,G.; Hussaini, S.M.A.; Sridhar, B.;Machiraju, P.K; Org. Biomol. Chem., 2015, 13, 1347.
  • Recent developments towards podophyllotoxin congeners as potential apoptosis inducers. Kamal, A.; Hussaini, S.M.A.; Malik, M.S.; Anti-Cancer Agents Med. Chem. 2015, 15, 565.
  • Hybrid pharmacophore design and synthesis of naphthalimide-benzimidazole conjugates as potential anticancer agents. Kamal, A; Kumar, P.P; Khan, M.N.A; Sheshadri, B.N; Srinivas, O; Letters in Drug Design & Discovery. 2015, 12, 374.
  • Dithiocarbamate/piperazine bridged pyrrolobenzodiazepines as DNA-minor groove binders: synthesis, DNA-binding affinity and cytotoxic activity.  Kamal, A.; Sreekanth, K.;Shankaraiah, N.; Sathish, M.; Nekkanti, S.;Srinivasulu, V.; Bioorg. Chem., 2015, 59, 23.
  • A carbohydrate approach for the formal total synthesis of (−)-aspergillide. C.;Srihari, P.; Krishna, N.H.; Sridhar, Y.; Kamal, A.; Beilstein J. Org. Chem., 2014, 10, 3122.
  • An expedient total synthesis of mupirocin. H, Srihari, P.; Krishna, N.H.; Sridhar, Y.; Raju, A.K.; Kamal, A.; RSC Adv., 2014,4, 37629.
  • Design, Synthesis and anticancer evaluation of tetrahydro-β-carboline-hydantoin hybrids. Shankaraiah, N.; Nekkanti, S.; Chudasama, K. J.; Senwar, K. R.; Sharma, P.; Jeengar, M. K.; Naidu, V.G.M.; Srinivasulu, V.; Kamal, A.,Bioorg. Med. Chem.Lett., 2014, 24, 5413.
  • Synthesis of 2-anilinopyridine dimers as microtubule targeting and apoptosis inducing agents.  Kamal, A; Hussaini, S.M.A.; Nayak, V.L.;  Malik, M.S.; Sucharitha, M.L.; Shaik, T.B.;Bioorg. Med. Chem., 2014, 22, 6755.
  • L-proline mediated synthesis of quinoxalines; evaluation of cytotoxic and antimicrobial activity.  Kamal, A.; Babu, K.S.; Faazil, S.; Hussaini, S.M.A.; Shaik, A.B.; RSC Adv., 2014, 4, 46369.
  • Design and synthesis of imidazo[2,1-b]thiazole-chalcone conjugates: microtubule destabilizing agents.  Kamal.A.; Balakrishna, M.; Nayak, V.L.; Shaik, T.B.; Faazil, S.; Nimbarte, V.D.; ChemMedChem., 2014, 9, 2766.
  • Synthesis and biological evaluation of imidazo[1,5-a]pyridine-benzimidazole hybrids as inhibitors of both tubulin polymerization and PI3/Akt pathway. Kamal, A.; Rao, A.V.S.; Nayak, V.L.; Reddy N.V.S.; Swapna, K.; Ramakrishn, G.; Mallika, A.; Org. Biomol. Chem., 2014, 12, 9864.
  • Chemical preservatives-based storage studies and ethanol production from juice of sweet sorghum cultivar, ICSV 93046. Kumar, C.G.; Rao, P.S.; Gupta, S.; Malapaka, J.; Kamal, A.; Sugar Tech., 2014, 17, 404.
  • Synthesis of imidazo[2,1-b][1,3,4]thiadiazole-chalcones as apoptosis inducing anticancer agents. Kamal, A.; Reddy, V.S.; Santosh, K.; Kumar, G.B.; Shaik, A.B.; Mahesh, R.; Chourasiya, S.S.;  Sayeed, I.B.; Kotamraju, S.; Med.Chem.Comm., 2014, 5, 1718.
  • Synthesis and biological evaluation of 1,2,3-triazole linked aminocombretastatin conjugates as mitochondrial mediated apoptosis inducers. Kamal, A.; Shaik, B.; Nayak, V.L.; Nagaraju, B.; Kapure, J.S.; Malik, M.S.; Shaik, T.B.; Prasad, B.; Bioorg. Med. Chem., 2014, 22, 5155.
  • Pyrazole-oxadiazole conjugates: Synthesis, antiproliferative activity and inhibition of tubulin polymerization. Kamal, A.; Shaik, A.B.; Sowjanya, P.; Reddy, V.S.; Kumar, G.B.; Soma, G.; Nagabhushana, A.; Rakesh, M.; Nishant, J.; Siva, K.V.; Org. Biomol. Chem., 2014, 12, 7993.
  • Asymmetric michael addition of ketones to nitroolefins: Pyrrolidinyl-oxazole-carboxamides as new efficientorganocatalysts. Kamal, A.; Sathish, M.; Srinivasulu, V.; Chetna, J.; Chandrasekha, K.; Shalini, N.; Yellaiah, T.; Shankaraiah, N; Org. Biomol. Chem., 2014, 12, 8008.
  • Design and synthesis of aminostilbene–arylpropenones as tubulin polymerization inhibitors. Kamal,A.; Kumar, G.B.; Polepalli, S.; Shaik, A.B.; Reddy, V.S.; Reddy, M.K.; Reddy, Ch.R.; Mahesh, R.;Kapure, J.S.; Jain, N.; ChemMedChem., 2014, 9, 2565.
  • Synthesis and biological evaluation of podophyllotoxin congeners as tubulin polymerization inhibitors. Kamal, A.; Reddy, T.S.; Polepalli, S.; Shalini, N.; Reddy, V.G.; Rao, A.V.S.;Jain, N.; Shankaraiah, N.; Bioorg. Med. Chem., 2014, 22, 5466
  • Synthesis of imidazothiadiazole-benzimidazole conjugates as mitochondrial apoptosis inducers.Kamal, A.; Swapna, P.; Vishnuvardhan, M.V.P.S.; Rao, M.P.; Mullagiri, K.; Nayak, L.; Bagul, C.;Med.Chem.Commun., 2014, 5, 1644
  • Tankyrase inhibitors as therapeutic targets for cancer. Kamal A.; Riyaz Sd.; Srivastava A.K.; Rahim A.; Current Topics in Med. Chem., 2014, 14, 1967.
  • Rapid access to novel 1,2,3-triazolo-heterocyclic scaffolds via tandem knoevenagel condensation/azide-alkyne 1,3-dipolar cycloaddition reaction in one pot.Maurya, R.A.; Adiyala, P.R.; Reddy, C.N.; Kapure, J.S.; Kamal, A.; ACS Combinatorial Science, 2014, 16, 466.
  • Synthesis and biological evaluation of 4-aza-2,3-dihydropyridophenanthrolines as tubulin polymerization inhibitors.Kamal, A.; Reddy, T.S.; Polepalli, S.; Paidakula, S.;Srinivasulu, V.; Reddy, V.G.; Jain, N.; Shankaraiah, N.; Bioorg. Med. Chem. Lett., 2014, 24, 3356.
  • Biotin-c10-AppCH2ppA is an effective new chemical proteomics probe for diadenosine polyphosphate binding proteins.Azhar, M.A.; Wright, M.; Kamal, A.; Nagy, J Miller, A.D.; Bioorg. Med. Chem. Lett., 2014, 24, 2928.
  • Highly diastereoselective synthesis of spiro[cyclopropane-1,3-indolin]-2-ones via catalyst-free cyclopropanation using ethyl diazoacetate.Maurya, R.A.; Reddy, C.N.; Mani, G.S.; Kapure, J.S.; Adiyala, P.R.; Nanubolu, J.B.; Singarapu, K.K.; Kamal, A.; Tetrahedron, 2014, 70, 4709.
  • Synthesis and evaluation of N-(1-Benzyl-1H-1,2,3-triazol-4-yl)methyl)nicotinamides as potential anticancer agents that inhibit tubulin polymerization. Kamal, A.; Reddy, N.V.S.; Nayak, V.L.;  Bolla, N.R.; Rao, AV.S.; Prasad, B.; Bioorg. Med. Chem., 2014, 22, 3465.
  • Phenyliodonium diacetate mediated arylation of benzothiazoles with substituted styrenes. Kamal, A.; Reddy, N.V.S.; Prasad, B.; Tetrahedron Lett., 2014, 55, 3972.
  • Synthesis and biological evaluation of cinnamido linked benzophenone hybrids as tubulin polymerization inhibitors and apoptosis inducing agents.Kamal, A.; Reddy, Ch.R.; Vishnuvardhan, M.V.P.S.; Mahesh, R.; Nayak, V.L.; Prabhakar, S.; Ramakrishna, S.; Bioorg. Med.Chem.Lett., 2014, 24, 2309.
  • Synthesis of a terphenyl substituted 4-aza-2,3-didehydropodophyllotoxin analogues as inhibitors of tubulin polymerization and apoptosis inducers. Kamal, A.; Tamboli, J.R.; Nayak, V.L.;Adil, S.F.; Vishnuvardhan, M.V.P.S.; Ramakrishna S.; Bioorg. Med. Chem., 2014, 22, 2714.
  • Synthesis and biological evaluation of imidazo [2,1-b][1,3,4]thiadiazole linked oxindole conjugates as potent tubulin polymerization inhibitors. Kamal, A.; Rao M.P.N.; Das P.; Swapna P.; Sowjanya P.;  Vijaykumar D.; Kishore M.; Jeshma K.; Nishant J.; ChemMedChem., 2014, 9, 1463.
  • Synthesis of stable, synthetic diadenosine polyphosphate analogues using recombinant histidine-tagged lysyl tRNA synthetase (LysU). Wright, M; Azar, M.A; Kamal, A.; Miller, A.D; Bioorg. Med. Chem. Lett., 2014, 24, 2346. 
  • Synthesis of b-carboline-benzimidazole conjugates using lanthanum nitrate as catalyst and their biological evaluation. Kamal, A.; Rao M.P.N.; Swapna P.; Srinivasulu V.; Chandrakant B.; Shaik A.B.; Kishore M.; Jeshma K.; Reddy V.S.; Vidyasagar K.; Narayana N.; Org. Biomol. Chem., 2014, 12, 2370. 
  • Apoptosis-inducing agents: a patent review. Kamal A.; Faazil S.; Malik, M. S.; Expert Opinion on Therapeutic Patents., 2014, 24, 339.
  • First total synthesis of the E- and Z-isomers of cytospolide-D. Kamal A.; Balakrishna M.; Reddy P.V,; Rahim A.; Tetrahedron: Asymm. 2014, 25, 148.
  • Synthesis and anticancer potential of benzothiazole linked phenylpyridopyrimidinones and their diones as mitochondrial apoptotic inducers. Kamal A.; Ashraf Md.; Vishnuvardhan M.V.P.S.; Faazil S.; Nayak V.L. Bioorg. Med. Chem. Lett., 2014, 24, 147.
  • Palladium-catalyzed aryl C-H activation and tandem ortho-hydroxylation/alkoxylation of 2-aryl benzimidazoles: Cytotoxicity and DNA binding studies. Kamal A.; Srinivasulu V.; Satish M.P.; Tangella Y.; Nayak V.L.; Rao M.P.N.; Shankaraiah N.; Nagesh N.; Asian J. Org. Chem., 2014, 3, 68.
  • Synthesis and biological evaluation of benzo[b]furans as inhibitors of tubulin polymerization and inducers of apoptosis. Kamal A.; Reddy N.V.S.; Nayak V.L.; Reddy V.S.; Prasad B.; Nimbarte V.D.; Srinivasulu V.; Vishnuvardhan M.V.P.S.; Reddy C.S.; Chem. Med. Chem., 2014, 9, 117.
  • Regio- and stereoselective synthesis of novel spiropyrrolidines through 1,3-dipolar cycloaddition reactions of azomethine ylides and 2-styrylquinazolin-4(3H)-ones. Maurya, R.A;Nayak, R; Reddy, G.S; Kapure, J.S; Nanubolu, J.B; Singarapu, K.K; Ajitha M.; Kamal, A; RSC Adv., 2014,4, 32303.
  • Synthesis, biological evaluation and molecular modeling of (E)-2-aryl-5-styryl-1,3,4-oxadiazole derivatives as acetylcholine esterase inhibitors. Kamal A.; Shaik A.B.; Reddy G.N.; Kumar C.G.; Joseph J.; Kumar G.B.; Purushotham U.; Sastry G.N.; MedicinalChemistry Research, 2014, 23, 2080.
  • Design and synthesis of C3-pyrazole/chalcone linked b-carboline hybrids: Antitopoisomerase I, DNA interactive and apoptosis inducing anticacner agents. Kamal A.; Srinivasulu V.; Nayak V.L.; Satish M.P.; Satish M.; Shankaraiah N.; Bagul C.; Reddy N.V.; Rangaraj N.; Nagesh N.; ChemMedChem, 2014, 19, 2084.
  • Production of melanin pigment from pseudomonas stutzeri isolated from red seaweed hypnea musciformis.Kamal A.; Kumar C.G.; Sahu N.; Reddy G.N.; Prasad R.B.N.; Nagesh N.; Letters in Applied Microbiology, 2013, 57, 295.
  • Synthesis and study of benzothiazole conjugatges in the control of cell prolifieration by modulating Ras/MEK/ERK-dependent pathway in MCF-7 cells. Kamal A.; Faazil S.; Ramaiah, M. J.; Ashraf Md.; Balakrishna, M.; Pushpavali, S.NC.V.L.; Nibedita P.; Pal-Bhadra M.; Bioorg. Med. Chem. Lett., 2013, 23, 5733.
  • Synthesis and biological evaluation of imidazopyridine-oxindole conjugates as microtubule targeting agents. Kamal A.; Reddy V.S.; Karnewar S.; Chourasiya S.S.; Shaik A.B; Nagabhushana A.; Kumar G.B.; Kishor C.; Addlagatta A.; Kotamraju S.; ChemMedChem, 2013, 8, 2015.
  • Quinazolino linked 4β-amidopodophyllotoxin conjugates regulate angiongenic pathway and control breast cancer proliferation. Kamal A.; Tamboli J.R.; Ramaiah M.J.; Adil S.F.; Pushpavalli S.N.C.V.L.; Ganesh R.; Sarma P.; Bhadra U.; Pal-Bhadra M.; Bioorg. Med. Chem., 2013, 21, 6414.
  • Anti-tubercular agents. Part 8: Synthesis, antibacterial and antitubercular activity of 5-nitrofuran based 1,2,3-triazoles.Kamal A.; Hussaini S.M.A.;  Faazil S.; Ashraf Md.; Poornachandra Y.; Reddy G.N.; Kumar C.G.; Khan I.A.; Bioorg. Med. Chem. Lett., 2013, 23, 6842.
  • Catalyst-free stereoselective cyclopropanation of electron dificient alkenes with ethyl diazoacetate. Kamal A.; Maurya R.A.; Kapure J.S.; Reddy P.; Srikanth P.S.; Chandrasekhar D.; RSC Adv., 2013, 3,15600.
  • Enhancing the shelf life of sweet sorghum (sorghum bicolor (L.) moench) juice through pasteurization while sustaining fermentation efficiency. Kamal A.; C.G. Kumar.; P.S. Rao.; Soma Gupta.; Jayalakshmi M.; Suguar Tech., 2013, 15, 328.
  • Copper oxide nanoparticles supported on graphene oxide catalyzed S-arylation: An efficient and ligand free synthesis of aryl sulfides. Kamal A.; Srinivasulu, V.; Murty, J.N.S.R.C.; Shankaraiah, N., Nagesh N.; Reddy T.S,; Rao, A.V.S, Advanced Synthesis & Catalysis. 2013, 355, 2297.
  • AlCL3-NaI assisted cleavage of polymer-bound esters with concomitant amine coupling and azido-reductive cyclization: Synthesis of pyrrolobenzodiazepine derivatives. Kamal A.; Prabhakar, S.; Shankaraiah, N.; Makandeya, N.; Reddy, P. V.; Srinivasulu, V.; Sathish, M, Tetrahedron Lett., 2013,54, 4435.
  • 4β-[4′-(1-(Aryl) urea)benzamid]podophylotoxins as DNA topoisomerase I and IIa inhibitors and apoptosis indusing agents. Kamal, A.; Suresh, P.; Ramaiah, M. J.; Redy, T. S.; Kapavarapu, R.K.; Imthiajali, S.; Redy, T. L.; Pushpavali, S.NC.V.L.; Shankaraiah, N.; Bhadra, M. P.,  Bioorg. Med. Chem., 2013, 21, 5198.
  • Synthesis and biological evaluation of diaryl ether linked DC-81 conjugates as potential anti-tumor agents.Kamal, A.; Viswanath, A.; Ramaiah, M. J.; Murthy, J.N.S.R.C.; Sultana, F., Ramakrishna, G., Bhadra, M. P., Anti-Cancer Agents Med. Chem., 2013, 13, 1590.
  • Synthesis, DNA binding ability and anticancer activity of 2-heteroaryl substituted benzimidazoles linked pyrrolo[2,1-c][1,4]benzodiazepppine conjugates.  Kamal, A.; Kumar, P. P.; Khan, M.N.A.; Seshadri, B. N.; Sreekanth, K., Med. Chem., 2013, 9, 651.
  • Purification and biochemical characterization of feruloyl esterases from Aspergillus Terreusi MTCC 11096. Kumar, C. G.; Kamle, A.; Kamal. A., Biotechnology Progress, 2013, 29, 924.
  • Synthesis of 1, 5-diarylpyrazoles as potential COX-2 inhibitors with nitric oxide releasing ability. Rao, B. N.; Muthuppalaniappan, M.; Dinavathi, S. S.; Viswanadha, S.; Bagul, C.; Srinivas, K.; Vakkalanka, S.K.V.S.; Atcha, K. R.; Kamal, A., Letters in Drug Design & Discovery., 2013, 10, 594.
  • Effect of micronutrient treatments in main and ratoon crops of sweet sorghum cultivar ICSV 93046 under tropical conditions. Rao, P. S.; Kumar, C. G.; Jayalakshmi, M.; Kamal, A.; Reddy, B.V.S., Sugar Tech, 2013 (DOI 10.1007/s 12355-012-0172). 
  • The first total synthesis of nhatrangin.  Kamal, A.; Reddy, V. S., Org. Biomol. Chem., 2013, 11, 4442. 
  • Synthesis of pyrazolo[1,5-a]pyrimidine linked aminobenzothiazole conjugates as potential anticancer agents. Kamal, A.; Tamboli, J. R.; Nayak, V. L.; Adil, S. F.; Vishnuvardhan, M.V.P.S.;Ramakrishna, S., Bioorg. Med. Chem. Lett., 2013, 23, 3208.
  • Anti-tubercular agents. part 7: A new class of diarylpyrrole-oxazolidinone conjugates as antimycobacterial agents. Kamal, A.; Swapna, P.; Shetti, R.V.C.R.N.C.; Shaik, A. B.; Rao, M.P.N.; Sultana, F.; Khan, I. A.; Sharma, S.; Kalia, N. P.; Kumar, S.; Chandrakant, B., Eur. J. Med. Chem., 2013, 64, 239.
  • An improved iron-mediated synthesis of N-2-aryl substituted 1,2,3-triazoles.Kamal, A.; Swapna, P., RSC Adv., 2013, 3, 7419.
  • The design and development of imidazothiazole-chalcone derivatives as potential anticancer drugs. Kamal, A.; Reddy, M. K.; Viswanath, A., Expert Opin. Drug Discov., 2013, 8, 289.
  • Naphthalimide derivatives with therapeutic characteristics: a patent review. Kamal, A.; Bolla, N. R.; Srikanth, P. S.; Srivastava, A. K., Expert Opin. Ther. Patents., 2013, 23, 299.
  • Metabolite profiling and biologoical activities of bioactive compounds produced by Chrysosporium lobatum strain BK-3 isolated from Kaziranga National Park, Assam, India. Kumar C. G.; Mongolla, P.; Sujitha, P.; Joseph, J.; Babu, K. S.; Suresh, G.; Ramakrishna, K. V. S.; Purushotham, U.; Sastry, G. N., Kamal, A., SpringerPlus., 2013, 2, 122.
  • Design, synthesis and biological evaluation of imidazo[1,5-a]pyridine-PBD conjugates as potential DNA-directed alkylating agents.  Kamal, A.; Ramakrishna, G.; Ramaiah, M. J.; Viswanath, A.; Rao, A.V.S.; Bagul, C.; Mukhopadyay, D.; Pushpavalli, S.N.C.V.L.; Bhadra, M. P.,  Med.Chem.Comm., 2013, 4, 697.
  • Synthesis and biological evaluation of new oxazolidino-sulfonamides as potential antimicrobial agents.Kamal, A.; Swapna, P.; Shetti, R.V.C.R.N.C.; Shaik, A. B.; Rao, M.P.N.; Gupta, S., Eur. J. Med. Chem., 2013, 62, 661.
  • 3-Diarylethyne quinazolinones: A new class of senescene inducers. Kamal, A.; Sultana, F.; Ramaiah, M. J.; Srikanth, Y.V.V.; Viswanath, A.; Bharathi, E. V.; Nayak, R.; Pushpavalli, S.N.C.V.L.; Srinivas, C.; Bhadra, M. P., Med.Chem.Comm., 2013 4, 575.
  • Synthesis of benzopyran linked pyrrolo[2,1-c][1,4]benzodiazepines as DNA-binding and potential anticancer agents. Kamal, A.; Rajender; Reddy, M. K.; Reddy, V. S.; Kumar, G. B., Medicinal Chemistry, 2013, 9, 177.
  • Synthesis and anticancer activity of heteroaromatic linked 4β-amido podophyllotoxins as apoptotic indusing agents.Kamal, A.; Tamboli, J. R.; Vishnuvardhan, M.V.P.S.; Adil, S. F.; Nayak, V. L.; Ramakrishna, S., Bioorg. Med. Chem. Lett., 2013, 23, 273.
  • Synthesis and biological evaluation of combretastatin-amidobenzothiazole conjugates as potential anticancer agents. Kamal, A.; Mallareddy, A.; Ramaiah, M. J.; Pushpavalli, S.N.C.V.L.; Suresh, P.; Kishor, C.; Murthy, J.N.S.R.C.; Rao, N. S.; Ghosh, S.; Anthony, A.; Bhadra, M. P., Eur. J. Med. Chem., 2012, 56, 166.
  • Synthesis of tetrazole-isoxazoline hybrids as a new class of tubulin polymerization inhibitors. Kamal, A.; Viswanath, A.; Ramaiah, M. J.; Murthy, J.N.S.R.C.; Sultana, F.; Ramakrishna, G.; Tamboli, J. R.; Pushpavalli, S.N.C.V.L.; Pal, D.; Kishor, C.; Anthony, A.; Bhadra, M. P., Med. Chem. Comm., 2012, 3, 1386.
  • Water mediated heck and ullmann couplings by supported palladium nanoparticles: Importance of surface polarity of the carbon spheres. Kamal, A.; Srinivasulu, V.; Seshadri, B. N.; Markandeya, N.; Alarifi, A.; Shankaraiah, N., Green Chemistry 2012, 14, 2513.
  • Anthranilamide-pyrazolo[1,5-a]pyrimidine conjugates as p53 activators in cervical cancer cells. Kamal, A.; Tamboli, J. R.; Ramaiah, M. J.; Adil, S. F.; Rao, G. K.; Viswanath, A.; Mallareddy, A.; Pushpavalli, S.N.C.V.L.; Bhadra, M. P., ChemMedChem., 2012, 7, 1453.
  • Inter and intrastrand DNA crosslinks by 2-fluoro-substituted pyrrolobenzodiazepine dimers: stability, stereochemistry and drug orientation. Seifert, J.; Pezeshki, S.; Kamal, A.; Weisz, K., Org. Biomol. Chem., 2012, 10, 6850.
  • Synthesis, biological evaluation of 5-carbomethoxymethyl-7-hydroxy-2-pentylchromone,5-carboethoxymethyl-4′,7-dihydroxyflavone and their analogues. Kamal, A.; Murty, J.N.S.R.C.; Viswanath, A.; Sujatha, P.; Kumar, C. G., Bioorg. Med. Chem.Lett., 2012, 22, 4891.
  • Synthesis of chalcone-amidobenzothiazole conjugates as antimitotic and apoptotic inducing agents. Kamal, A.; Mallareddy, A.; Suresh, P.; Shaik, T. B.; Nayak, V. L.; Kishore, C.; Shetti, R.V.C.R.N.C.; Rao, N. S.; Tamboli, J. R.; Ramakrishna, S.; Anthony, A., Bioorg. Med. Chem., 2012, 20, 3480.
  • Recent advances on structural modifications of benzothiazoles and their conjugate systems as potential chemotherapeutics. Kamal, A.; Srikanth, Y.V.V.; Khan, M.N.A.; Sultana, F.; Reddy, M. K., Expert Opin. Investig. Drugs., 2012, 21, 619.
  • Interaction of pyrrolobenzodiazepine (PBD) ligands with parallel intermolecular G-quadruplex complex using spectroscopy and ESI-MS. Raju, G.; Srinivas, R.; Reddy, V. S.; Idris, M. M.; Kamal, A.; Nagesh, N., PloS ONE, 2012, 7, e35920.
  • Feasibility of sustaining sugars in sweet sorghum stalks during post-harvest stage by exploring cultivars and chemicals: A desk study. Rao, P. S.; Kumar, C. G.; Malapaka, J.;  Kamal, A., Reddy, B.V.S., Sugar Tech., 2012, 14, 21.
  • p53-Mdm2 Inhibitors: Patent review (2009-2010). Kamal, A.; Azhar, M. A.; Shaik, T. B., Expert Opinion on Therapeutic Patents 2012, 22, 95.
  • Synthesis of terphenyl benzimidazoles as tubulin polymerization inhibitors.Kamal, A.; Reddy, M. K.; Shaik, T. B.; Rajendar; Srikanth, Y.V.V.; Reddy, V. S.; Kumar, G. B.; Kalivendi, S. V., Eur. J. Med. Chem., 2012, 50, 9.
  • Synthesis and biological evaluation of 4β-sulphonamido and 4β-[(4'-sulphonamido)benzamide]podophyllotoxins as DNA topoisomerase-IIa and apoptosis inducing agents.Kamal, A.; Suresh, P.; Ramaiah, M. J.; Mallareddy, A.; Imthiajali, S.; Pushpavalli, S.N.C.V.L.; Lavanya, A.; Bhadra, M. P., Bioorg. Med. Chem., 2012, 20, 2054.
  • 3-Substituted 2-phenylimidazo[2,1-b]benzothiazoles: Synthesis, anticancer activity and inhibition of tubulin polymerization. Kamal, A.; Sultana, F.; Ramaiah, M. J.; Srikanth, Y.V.V.; Viswanath, A.; Kishore, C.; Sharma, P.; Pushpavalli, S.N.C.V.L.; Anthony, A.; Bhadra, M. P., Chem. Med. Chem., 2012, 7, 292.
  • Synthesis, anticancer activity and inhibition of tubulin polymerization of bisindole sulfonates. Kamal, A.; Srikanth, Y.V.V.; Khan, M.N.A.; Ashraf, Md.; Shaik, T. B.; Kalivendi, S. V., Letters in Drug Design & Discovery  2012, 9, 242.
  • Synthesis, DNA binding and anticancer activity of pyridylimidazolidinone linked pyrrolo[2,1-c][1,4]benzodiazepine conjugates. Kamal, A.; Kumar, B. A.; Suresh, P., Letters in Drug Design & Discovery 2012, 9, 234.
  • Synthesis and anticancer activity of 4β-alkylamidochalcone and 4β-cinnamido linked podophylotoxins as apoptotic inducing agents. Kamal, A.; Mallareddy, A.; Suresh, P.; Nayak, V. L.; Shetti, R.V.C.R.N.C.; Rao, N. S.; Tamboli, J. R.; Shaik, T. B.; Vishnuwardhan, M.V.P.S.; Ramakrishna, S., Eur. J. Med. Chem. 2012, 47, 530.
  • Design and synthesis of benzo[c,d]indolone-pyrrolobenzodiazepine conjugates as potential anticancer agents. Kamal, A.; Ramakrishna, G.; Nayak, V. L.; Raju, P.; Rao, A.V.S.; Viswanath, A.; Vishnuwardhan, M.V.P.S.; Ramakrishna, S.; Srinivas, G., Bioorg. Med. Chem., 2012, 20, 789.
  • Metabolic profiling and biological activities of bioactive compounds produced by Pseudomonas sp. strain ICTB-745 isolated from Ladakh, India. Kamal, A.; Shaik, A. B.; Kumar, C. G.; Mongolla, P.; Rani, P. U.; Krishna, K.V.S.R.; Mamidyala, S. K.; Joseph, J., J. Microbiol. Biotechnol., 2012, 22(1), 69.
  • Synthesis, anticancer activity and apoptosis inducing ability of bisindole linked pyrrolo[2,1-c][1,4]benzodiazepine conjugates. Kamal, A.; Srikanth, Y.V.V.; Ramaiah, M. J.; Khan, M. N. A.; Reddy, M. K., Ashraf, Md.; Lavanya, A.; Pushpavalli, S.N.C.V.L.; Bhadra, M. P.,Bioorg. Med. Chem. Lett., 2012, 22, 571.
  • Isolation and identification of diadenosine 5′,5′′-P1,P4-tetraphosphate binding proteins using magnetic bio-panning. Guo, W.; Azhar, M.A.; Xu, Y.; Wright, M.; Kamal, A.; Miller, A. D., Bioorg. Med. Chem. Lett., 2011, 21, 7175.
  • Synthesis and apoptosis inducting ability of new anilino substituted pyrimidine sulphonamides as potential anticancer agents. Kamal, A.; Dastagiri, D.; Ramaiah, M. J.; Reddy, J. S.; Bharathi, E. V.; Reddy, M. K.; Sagar, M.V.P.; Reddy, T.L.; Pushpavalli, S.N.C.V.L.; Bhadra, M. P., Eur. J. Med. Chem. 2011,46, 5817.
  • 2-Anilinonicotinyl linked 2-aminobenzothiazoles and [1,2,4]triazolo[1,5-b][1,2,4] benzothiadiazine conjugates as potential mitochondrial apoptotoc inducers. Kamal, A.; Srikanth, Y.V.V.; Khan, M.N.A.; Ashraf, Md.; Reddy, M. K.;Sultana, F.; Kaur, T.; Chashoo, G.; Suri, N.; Sehar, I.; Wani, Z. A.; Saxena, A.; Sharma, P. R.; Bhushan, S.; Mondhe, D. M.; Saxena, A. K., Bioorg. Med. Chem., 2011, 19, 7136.
  • Synthesis of cinnamide dimers as potential antibacterial and antifungal agents. Kamal, A.; Ramakrishna, G.; Raju, P.; Rao, A.V.S.; Joseph, J.; Siddhardha, B.; Murthy, U.S.N., Lett. in Drug Design & Discovery, 2011, 8, 957.
  • A one-pot azido reductive tandem mono-N-alkylation employing dialkylboron triflates: Online ESI-MS mechanistic investigation. Shankaraiah, N.; Markandeya, N.; Srinivasulu, V.; Sreekanth, K.; Reddy, Ch. S.; Santos, L. S.; Kamal, A.;J. Org. Chem., 2011, 76, 7017.
  • Synthesis and anticancer activity of chalcone-pyrrolobenzodiazepine conjugates linked via 1,2,3-triazole ring side-armed with alkane spacers. Kamal, A.; Prabhakar, S.; Ramaiah, M. J.; Reddy, P. V.; Reddy, Ch. R.; Mallreddy, A.; Shankaraiah, N.; Reddy, T. L. N.; Pushpavalli, S.N.C.V.L.; Bhadra, M. P., Eur. J. Med. Chem., 2011, 46, 3820.
  • Synthesis of aryl-substituted naphthalene-linked pyrrolobenzodiazepine conjugates as potential anticancer agents with apoptosis-inducing ability.  Kamal, A.; Reddy, M. K.; Ramaiah, M. J.; Srikanth, Y.V.V.; Rajendar; Reddy, V.S.; Kumar, G. B.; Pushpavalli, S.N.C.V.L.; Bag, I.; Juvekar, A.; Sen, S.;Zingde, S. M.  ; Bhadra, M. P., ChemMedChem., 2011¸6¸ 1665.
  • 2-Anilinonicotinyl linked 1,3,4-oxadiazole derivatives: Synthesis, antitumour activity and inhibition of tubuline polymerization. Kamal, A.; Srikanth, Y.V.V.; Shaik, T. B.; Khan, M.N.A.; Ashraf, Md.; Reddy M. K.; Kumar, K. A.; Kalivendi, S. V., Med. Chem. Comm., 2011,2, 819.
  • Synthesis and biological evaluation of conformationally flexible as well as restricted dimers of monastrol and related dihydropyrimidones. Kamal, A.; Malik, M. S.; Bajee, S.; Azeeza, S.; Faazil, S.; Ramakrishna, S.; Naidu, V.G.M.; Vishnuwardhan, M. V. P. S., Eur. J. Med. Chem., 2011,46, 3274.
  • Carbazole-pyrrolo[2,1-c][1,4] benzodiazepine conjugates: design, synthesis, and biological evaluation. Kamal, A.; Shetti, R.V.C.R.N.C.; Ramaiah, M. J.; Swapna, P.; Reddy, K. S.; Mallareddy,A.; Rao, M. P. N.; Chourasia, M.; Sastry, G. N.; Juvekar, A.; Zingde, S.; Sarma, P.; Pushpavalli, S.N.C.V.L.; Bhadra, M. P., Med. Chem. Comm., 2011, 2, 780.
  • Synthesis and anticancer activities of new benzothiadiazinyl hydrazine-carboxamides and aniline[1,2,4]triazolo[1,5-b][1,2,4]thiadiazine 5,5-diones. Kamal, A.; Srikanth, Y.V.V.; Ashraf, Md.; Khan, M.N.A.; Shaik, T. B.; Kalivendi, S. V.; Suri, N.; Saxena, A. K.,Med. Chem.Comm., 2011, 7, 165.
  • Chalcone-imidazolone conjugates induce apoptosis through DNA damage pathway by affecting telomeres. Ramaiah, M. J.; Pushpavalli, S.N.C.V.L.; Krishna, G. R.; Sarma, P.; Mukhopadhyay, D.; Kamal, A.; Bhadra, U.; Bhadra, M. P., Cancer Cell International, 2011, 11, 11.
  • Synthesis and anticancer activity of oxindole derived imidazo[1,5-a]pyrazines. Kamal, A.; Ramakrishna, G.; Raju, P.; Rao, A. V. S.; Viswanadh, A.; Nayak, V. L.; Ramakrishna, S., Eur. J. Med. Chem. 2011, 46, 2427.
  • Synthesis and biological evaluation of 4β-acrylamidopodophyllotoxin congeners as DNA damaging agents. Kamal, A.; Suresh, P.; Ramaiah, M. J.; Mallareddy, A.; Kumar, B. A.; Raju, P.; Gopal, J. V.; Pushpavalli, S.N.C.V.L.; Lavanya, A.; Sarma, P.; Bhadra, M. P., .Bioorg. Med. Chem., 2011, 19, 4589.
  • Synthesis of 4ß-carbamoyl epipodophyllotoxins as potential antitumour agents. Kamal, A.; Kumar, B. A.; Suresh, P.; Juvekar, A.; Zingde, S., Bioorg. Med. Chem., 2011, 19, 2975.
  • Synthesis and biological evaluation of  linked pyrrolo[2,1-c][1,4] benzodiazepine (PBD) conjugates as potential anticancer agents. Kamal, A.; Reddy, M. K.; Ramaiah, M. J.; Rajender; Reddy, J. S.; Srikanth, Y. V. V.; Dastagiri, D.; Bharathi, E. V.; Pushpavalli, S.N.C.V.L.; Sarma, P.; Bhadra, M. P., Bioorg. Med. Chem., 2011, 19, 2565.
  • Synthesis of a new 4-aza-2,3-didehydropodophyllotoxin analogues as potent cytotoxic and antimitotic agents. Kamal, A.; Suresh, P.; Mallareddy, A.; Kumar, B. A.; Reddy, P. V.; Raju, P.; Tamboli, J. R.; Shaik, T. B.; Jain, N.; Shashi, V. K., Bioorg. Med. Chem., 2011, 19, 2349.
  • Anti-tubercular agents, Part 6: Synthesis and antimycobacterial activity of novel arylsulfonamido conjugated oxazolidinones. Kamal, A.; Shetti, R.V.C.R.N.C.; Azeeza, S.; Swapna, P.;Khan, M.N.A.; Khan, I. A.; Sharma, S.; Abdullah, S. T., Eur. J. Med. Chem., 2011, 46, 893.
  • Novel synthesis of stagonolide-F, putaminoxin and aspinolide-A. Kamal, A.; Reddy, P. V.; Balakrishna, M.; Prabhakar, S., Lett. in Org. Chem., 2011, 8, 143.
  • Investigations of microbial resistance among bacteria dwelling in Indian soils. Kumar, C. G.; Joseph, J.; Kamal, A., Current Trends in Biotechnology and Pharmacy, 2011, 5, 1049.
  • Decolorization and biotransformation of triphenylmethane dey, methyl violet, by aspergillus sp. isolated from Ladakh, India. Kumar, C. G.; Mongolla, P.; Basha, A.; Joseph, J.; Sarma, V. U. M.; Kamal, A., J. Microbiol. Biotechnol., 2011, 21, 267.
  • Optimization of nitrilase production from alcaligenes faecalis IICT-A3: effect of inducers on substrate specificity. Nageswar. Y.V.D.; Sheelu, G.; Shambhu, R. R.; Hemalatha, M.; Mehdi, N.; Malik, M. S.; Kamal, A., Bioprocess and Biosystems Engineering, 2011, 34, 515.
  • Total synthesis of rutaecarpine and analogues by tandem azido reductive cyclization assisted by microwave irradiation. Kamal, A.; Reddy, M. K.; Reddy, T. S.; Santos, L. S.; Shankaraiah, N., Synlett 2011, 1, 0061
  • Synthesis and biological evaluation of 3, 5-diaryl isoxazoline/isoxazole linked 2,3-dihydroquinazolinone hybrids as anticancer agents. Kamal, A.; Bharathi, E. V.; Reddy, J. S.; Ramaiah, M. J.; Dastagiri, D.; Reddy, M. K.; Viswanadh, A.; Reddy, T. L.; Shaik, T. B.; Pushpavalli, S.N.C.V. L.; Bhadra, M. P., Eur. J. Med. Chem., 2011, 46, 691.
  • An expedient total synthesis of optically active piperidine and indolizidine alkaloids (-)-β-conhydrine and (-)-lentiginosine. Kamal, A.; Reddy, V. S., Tetrahedron 2011, 67, 1341.
  • An efficient one-pot synthesis of benzothiazolo-4β-anilino-podophyllotoxin congeners: DNA topoisomerase-II inhibition and anticancer activity. Kamal, A.; Kumar, B. A.; Suresh, P.; Shankaraiah, N.; Kumar, M. S., Bioorg. Med. Chem. Lett., 2011, 21, 350.
  • Characterization of improved sweet sorghum genotypes for biochemical parameters, sugar yield and its attributes at different phonological stages. Kumar, C. G.; Fatima, A.; Rao, P. S.; Reddy, B.V.S.; Rathor, A.; Rao, R. N.; Khalid, S.; Kumar, A. A.; Kamal, A., Sugar Tech., 2010, 12, 322.
  • Bioconversion of acrylonitrile to acrylic acid by Rhodococcus ruber strain AKSH-84. Kamal, A.; Kumar, M. S.; Kumar, C. G.; Shaik, T. B., J. Microbiol. Biotechnol., 2010, 21(1), 37.
  • Design, synthesis and biological evaluation of imidazopyridine/ pyrimidine-chalcone derivatives as potential anticancer agents. Kamal, A.; Reddy, J. S.; Ramaiah, M. J.; Dastagiri, D.; Bharathi, E. V.; Sagar, M. V. P.; Pushpavalli, S.N.C.V.L.; Ray, P.; Bhadra, M. P., Med. Chem. Comm., 2010, 1, 355.
  • Asymmetric syntheses of piperidino-benzodiazepines through ‘cation-pool’ host/guest supramolecular approach and their DNA-binding studies. Markandeya, N.; Shankaraiah; N., Reddy, Ch. S.; Santos, L. S.; Kamal, A.; Tetrahedron: Asymm. 2010, 21, 2625.
  • Antimicrobial activity from the extracts of fungal isolates of soil and dung samples from Kaziranga National Park, Assam, India. Kumar, C. G.; Mongolla, P.; Joseph, J.; Nageswar, Y.V.D.; Kamal, A., J. Mycologie Medicale 2010, 20, 283.
  • Synthesis of 4β-N-polyaromatic substituted podophyllotoxins: DNA topoisomerase inhibition, anticancer and apoptosis-inducing activities. Kamal, A.; Kumar, B. A.; Suresh, P.; Agarwal, S. K.; Chashoo, G.; Singh, S. K.; Saxena, A. K., Bioorg. Med. Chem., 2010, 18, 8493.
  • An efficient synthesis of synargentolide A from D-mannitol. Kamal, A.; Balakrishna, M.; Reddy, P. V.; Faazil, S., Tetrahedron: Asymm., 2010, 21, 2517.
  • Synthesis of imidazothiazole-chalcone derivatives as anticancer and apoptosis inducing agents.  Kamal, A.; Dastagiri, D.; Ramaiah, M. J.; Reddy, J. S.; Bharathi, E. V.; Srinivas, C.; Pushpavallil, S.N.C.V.L.; Pal, D.; Bhadra, M. P., Chem.Med.Chem., 2010, 5, 1937.
  • Synthesis of cyclodextrin derivatives of amino-(thiazolyl) coumarins as potential antimicrobial agents. Kamal, A.; Adil, S. F.; Tamboli, J. R.; Siddardha, B.; Murthy, U.S.N., Letters in Drug Design & Discovery 2010, 7, 665.
  • Anti-tubercular agents. Part 5: Synthesis and biological evaluation of benzothiadiazine 1,1-dioxide based congeners. Kamal, A.; Shetti, R.V.C.R.N.C.; Azeeza, S.; Ahmed, S. K.; Swapna, P.; Reddy, A. M.; Khan, I. A.; Sharma, S.; Abdullah, S. T.,  Eur. J. Med. Chem. 2010, 45, 4545.
  • Synthesis, anticancer activity and mitochondrial mediated apoptosis inducing ability of 2,5-diaryloxadiazole-pyrrolobenzodiazepine conjugates. Kamal, A.; Dastagiri, D.; Ramaiah, M. J.; Bharathi, E. V.; Reddy, J. S.; Balakishan, G.; Sarma, P.; Pushpavallil, S.N.C.V.L Bhadra, M. P.; Juvekar, A.; Sen, S.; Zingde, S.,  Bioorg. Med. Chem. 2010, 18, 6666.
  • Synthesis of 3,3-diindolyl oxyindoles efficiently catalyzed by FeCL3 and their in vitro evaluation for aniticancer activity. Kamal, A.; Srikanth, Y.V.V.; Khan, M. N. A.; Shaik, T. B.; Ashraf, Md., Bioorg. Med. Chem. Lett. 2010, 20, 5229.
  • Synthesis and biological evaluation of anilino substituted pyramidine linked pyrrolobenzodiazepines as potential anticancer agents. Kamal, A.; Reddy, J. S.; Ramaiah, M. J.; Bharathi, E. V.; Dastagiri, D.; Reddy, M. K.; Pushpavallil, S.N.C.V.L .; Bhadra, M. P., Bioorg. Med. Chem. Lett. 2010, 20, 5232.
  • Synthesis and anticancer activity of chalcone linked imidazolones. Kamal, A.; Ramakrishna, G.; Raju, P.; Viswanath, A.; Ramaiah, M. J.; Balakrishna, G.; Bhadra, M. P., Bioorg. Med. Chem. Lett. 2010, 20, 4865.
  • NMR structural studies on the covalent DNA binding of a pyrrolobenzo-diazepine-naphthalimide conjugates. Rettig, M.; Langel, W.; Kamal, A.; Weisz, K., Org. Biomol. Chem.2010, 8, 3179.
  • Synthesis and biological evaluation of cinnamido linked pyrrolo[2,1-c][1,4]benzodiazepines as antimitotic agents. Kamal, A.; Balakrishna, G.; Ramakrishna, G.; Shaik, T. B.;  Sreekanth, K.; Balakrishna, M.; Rajender; Dastagiri, D.;  Shashi, V. K., Eur. J. Med. Chem. 2010, 45, 3870.
  • Design, synthesis and biological evaluation of 3,5-diarylisoxazoline/ isoxazole-pyrrolobenozodiazepine conjugates as potential anticancer agents. Kamal, A.; Reddy, J. S.; Ramaiah, M. J.; Dastagiri, D.; Bharathi, E. V.; Bhadra, M. P.; Juvekar, A.,Eur. J. Med. Chem. 2010, 45, 3924.
  • Search for new & novel chemotherapeutics for the treatment of human malignancies. Kamal, A.; Azeeza, S.; Bharathi, E. V.; Malik, M. S.; Shetti, R.V.C.R.N.C., Mini-Reviews in Medicinal Chemistry 2010, 10, 405.
  • Synthesis of bis-1,2,3-triazolo-bridged unsymmetrical pyrrolobenzodiazepine trimers via ‘click’ chemistry and their DNA-binding studies. Kamal, A.; Shankaraiah, N.; Reddy, Ch. R.; Prabhakar, S.; Markandeya, N.; Srivastava, H. K.; Sastry, G. N., Tetrahedron  2010, 66, 5498.
  • Synthesis, DNA-binding ability and anticancer activity of benzothiazole/benzoxazole-pyrrolo[2,1-c][1,4]benzodiazepine conjugates. Kamal, A.; Reddy, K. S.; Khan, M.N.A.; Shetti, R.V.C.R.N.C.; Ramaiah, M. J.; Pushpavallil, S.N.C.V.L.; Srinivas, C.; Bhadra, M. P.; Chourasia, M.; Sastry, G. N.; Juvekar, A.; Zingde, S.; Barkume, M.,   Bioorg. Med. Chem. 2010, 18, 4747.
  • Synthesis, anticancer activity and apoptosis inducing ability of anthranilamide-PBD conjugates. Kamal, A.; Bharathi, E. V.; Ramaiah, M. J.; Reddy, J. S.; Dastagiri, D.; Viswanath, A.; Sultana, F.; Pushpavallil, S.N.C.V.L.; Bhadra, M. P., Juvekar, A.; Sen, S.; Zingde, S., Bioorg. Med. Chem. Lett. 2010, 20, 3310.
  • Synthesis and potential cytotoxic activity of new phenanthrylphenol-pyrrolobenzodiazepines. Kamal, A.; Sreekanth, K.; Kumar, P. P.; Shankaraiah, N.; Balakrishna, G.; Ramaiah, M. J.; Pushpavalli, S.N.C.V.L.; Ray, P.; Bhadra, M. P., Eur. J. Med. Chem. 2010, 45, 2173.
  • New therapeutics: Potential for drug resistant tuberculosis. Kamal, A.; Azeeza, S.; Malik, M. S.; Faazil, S., International Journal of Medical and Biological Frontiers 2010, 535.
  • Quinazolinone linked pyrrolo[2,1-c][1,4]benzodiazepine (PBD) conjugates: Design, synthesis and biological evaluation as potential anticancer agents. Kamal, A.; Bharathi, E. V.; Ramaiah, M. J.; Dastagiri, D.; Reddy, J. S.; Viswanath, A.; Sultana, F.; Pushpavallil, S.N.C.V.L.; Bhadra, M. P., Srivastava, H. K.; Sastry, G. N.; Juvekar, A.; Sen, S.; |Zingde, S., Bioorg. Med. Chem. 2010, 18, 526.
  • Solution structure of a covalently bound pyrrolo[2,1-c][1,4] benzodiazepine-benzimidazole hybrid to a 10mer DNA duplex. Rettig, M.; Weingarth, M.; Langel, W.; Kamal, A.; Kumar, P. P.; Weisz, K., Biochemistry 2009, 48, 12223.
  • An efficient aldol-based approach for the synthesis of dihydrokawain-5-ol. Kamal, A.; Reddy, P. V.; Prabhakar, S., Tetrahedron: Asymm. 2009, 20, 1936.
  • Total synthesis of aculeatins A and B from (S)-malic acid. Kamal, A.; Reddy, P. V.; Prabhakar, S.; Balakrishna, M., Tetrahedron: Asymm. 2009, 20, 2861.
  • Stereoselective total synthesis of (+)-b-conhydrine from D-mannitol. Kamal, A.; Reddy, V. S.; Reddy, N.V.S.; Reddy, V. S., Tetrahedron: Asymm. 2009, 20, 2589.
  • Stereoselective total synthesis of simplactone A. Kamal, A.; Reddy, P. V.; Prabhakar, S.; Suresh, P., Tetrahedron: Asymm. 2009, 20, 1798.
  • Synthesis of coumarin linked naphtalimide conjugates as potential anticancer and antimicrobial agents. Kamal, A.; Adil, S. F.; Tamboli, J. R.; Siddardha, B.; Murthy, U.S.N., Letters in Drug Design & Discovery, 2009, 6, 201.
  • Chemoselective aromatic azido reduction with concomitant aliphatic azide employing Al/Gd triflates-NaI and ESI-MS mechanistic studies. Kamal, A.; Markandeya, N.; Shankaraiah, N.; Reddy, Ch. R.; Prabhakar, S.; Reddy, C. S.; Eberlin, M. N.; Santos, L. S.,Chemistry-A European Journal, 2009, 15, 7215.
  • One-pot microwave-assisted selective azido reduction/tandem cyclization in condensed and solid phase with nickel boride. Shankaraiah, N.;Markandeya, N; Espinoza-Moraga, M.; E.M.; Arancibia, C.; Kamal, A.; Santos, L.S., Synthesis, 2009, 13, 2163.
  • Total synthesis of (R)- and (S)-turmerone and (7S,9R)-bisacumol by an efficient chemoenzymatic approach. Kamal, A.; Malik, M. S.; Azeeza, S.; Bajee, S.; Shaik, A. A., Tetrahedron: Asymm. 2009, 20, 1267.
  • Remarkable enhancement in the DNA-binding ability of C2-fluoro substituted pyrrolo[2,1-c][1,4]benzodiazepines and their anticancer potential.Kamal, A.; Rajender; Reddy, D. R.; Reddy, M. K.; Balakrishna, G.; Shaik, T. B.; Chourasia, M.; Sastry, G. N., Bioorg. Med. Chem., 2009, 17, 1557.
  • An efficient synthesis of bis(indolyl) methanes and evaluation of their antimicrobial activities. Kamal, A.; Khan, M.N.A.; Reddy, K. S.; Srikanth, Y.V.V.; Ahmed, S. K.; Kumar, K. P.; Murthy, U.S.N., J. Enzyme Inhbn. & Med. Chem. 2009, 24, 559.
  • Synthesis and biological evaluation of mercapto triazolo-benzothiadiazine linked aminobenzothiazoles as potential anticancer agents. Kamal, A.; Khan, M.N.A.; Srikanth, Y.V.V.; Shetti, R.V.C.R.N.C., Chem. Bio. Drug Design, 2009, 73, 687.
  • Total synthesis of phytotoxic herbarumin-I from D-mannitol. Kamal, A.; Reddy, P. V.; Prabhakar, S., Tetrahedron: Asymm. 2009, 20, 1120.
  • Lipase mediated resolution of g-azidoalcohols in aqueous and organic media: Synthesis of (R)- and (S)- fluoxetine and duloxitine. Kamal, A.; Malik, M. S.; Shaik, A. A.; Azeeza, S., J. Mol. Cat. B: Enzymatic, 2009, 58, 132.
  • Spectroscopic and calorimetric studies on the DNA recognition of pyrrolo[2,1-c][1,4]benzodiazepine hybrids. Rettig, M.; Kamal, A.; Ramu, R.; Mikolajczak, J.; Weisz, K., Bioorg. Med. Chem. 2009, 17, 919.
  • Al(OTf)3 highly efficient catalyst for the tetrahydropyranylation of alcohols under solvent-free conditions. Kamal, A.; Khan, M.N.A.; Srikanth, Y.V.V.; Reddy, K. S., Can. J. Chem. 2008, 86, 1099.
  • Synthesis, DNA-binding ability and biological activity of C8 linked G1 dendrimer-pyrrolobenzodiazepine conjugates as anticancer agents. Kamal, A.; Balakrishna, G.; Rajender; Sreekanth, K.; Reddy, D. R.; Reddy, M. K., Sen, S.; Kurian, N.; Juvekar, A. S.; Zingde, S. M., Letters in Drug Design & Discovery, 2008, 5, 424.
  • Remarkable DNA binding affinity and potential anticancer activity of pyrrolo   [2,1-c][1,4]benzodiazepine napthalimide conjugates linked through piperazine side-armed alkane spacers. Kamal, A.; Ramu, R.; Tekumalla, V.; Khanna, G. B. R.; Barkume, M. S.; Juvekar, A. S.; Zingde, S. M., Bioorg. Med. Chem., 2008, 16, 7218.
  • Efforts towards the development of new antitubercular agents: Potential for thiolactomycin based compounds. Kamal, A.; Azeeza, S.; Malik, M. S.; Shaik, A. A.; Rao, M. V., J. Pharm Pharmaceut. Sci., 2008, 11, 106.
  • Synthesis, DNA-binding ability and evaluation of antitumour activity of triazolo[1,2,4]benzothiadiazine linked pyrrolo[2,1-c][1,4]benzodiazepine conjugates. Kamal, A.; Khan, M.N.A.; Srikanth, Y.V.V.; Reddy, K. S.; Juvekar, A. S.; Sen, S.; Kurian, N.; Zingde, S. M., Bioorg. Med. Chem. Lett. 2008, 16, 7804.
  • Synthesis and biological evaluation of a new series of benzothiazole-quinolone hybrids as antibacterial agents. Kamal, A.; Ahmed, S. K.; Khan, M.N.A.; Shetti, R.V.C.R.N.C.; Siddardha, B.; Murthy, U.S.N., Letters in Drug Design & Discovery 2008, 5, 353.
  • Synthesis and anticancer activity of pthalimido and naphthalimido substituted dihydropyrimidone conjugates. Kamal, A.; Adil, S. F.; Tamboli, J. R.; Siddardha, B.; Murthy, U.S.N., Letters in Drug Design & Discovery 2008, 5, 261.
  • Pyrrolo[2,1-c][1,4]benzodiazepine-b-glucuronide prodrugs with a potential for selective therapy of solid tumors by PMT and ADEPT strategies. Kamal, A.; Tekumalla, V.; Raju,  P.; Naidu, V.G.M.; Diwan, P. V.; Ramakrishna, S., Bioorg. Med. Chem. Lett. 2008, 18, 3769.
  • Synthesis of enantiomerically pure g-azidoalcohols by lipase-catalyzed transesterification, Kamal, A.; Malik, M. S.; Shaik, A. A.; Azeeza, S., Tetrahedron: Asymm. 2008, 19, 1078.
  • An efficient selective reduction of aromatic azides to amines employing BF3.Oet2/NaI: synthesis of pyrrolobenzodiazepines. Kamal, A.; Shankaraiah, N.; Markandeya, N.; Reddy, Ch. S., Synlett 2008, 9, 1297.
  • Lipase-catalyzed resolution of 1-chloro-3-[(4-morpholin-4-yl-1, 2, 5-thiadiazole-3-yl)oxy]propan-2-ol. Synthesis of (R)- and (S)-timolol. Kamal, A.; Krishnaji, T.; Khan, M.N.A., J. Mol. Cat.B: Enzymatic 2008, 54, 55.
  • Development of pyrrolo[2,1-c][1,4] benzodiazepine b-galactoside prodrugs for selective therapy of cancer by ADEPT and PMT. Kamal, A.; Venkatesh, T.; Krishnan, A.; Bhadra, M. P.; Bhadra, U., ChemMedChem 2008, 3, 794.
  • Synthesis of C8-C8/C-2-C8-linked triazolo pyrrolobenzodiazepine dimers by employing ‘click’ chemistry and their DNA-binding affinity. Kamal, A.; Prabhakar, S.; Shankariah, N.; Reddy, Ch. R.; Reddy, P. V., Tetrahedron Lett. 2008, 49, 3620.
  • Phosphonate linked pyrrolo[2,1-c][1,4]benzodiazepine conjugates: Synthesis, DNA binding affinity and cytotoxicity. Kamal, A.; Kumar, P. P.; Seshadri, B. N.; Srinivas, O.; Kumar, M. S.; Sen, S.; Kurian, N.; Juvekar, A. S.; Zingde, S. M.,Bioorg. Med. Chem. 2008, 16, 3895.
  • Synthesis of new benzimidazole linked pyrrolo[2,1-c]benzodiazepine conjugates with efficient DNA binding affinity and potent cytotoxicity.  Kamal, A.; Kumar, P. P.; Sreekanth, K.; Seshadri, B. N., Bioorg. Med. Chem. Lett. 2008, 18, 2594.
  • Solid-phase synthesis of new pyrrolobenzodiazepine-chalcone conjugates: DNA-binding affinity and anticancer activity. Kamal, A.; Shankaraiah, N.; Prabhakar, S.; Reddy, Ch. R.;Markandeya, N.;Reddy, K. L.; Devaiah, V., Bioorg. Med. Chem. Lett. 2008, 18, 2434.
  • Approaches based on enzyme mediated kinetic to dynamic kinetic resolutions: A versatile route for chiral intermediates. Kamal, A.; Azhar, M. A.; Krishnaji, T.; Malik, M. S.; Azeeza, S., Coord. Chem. Rev. 2008, 252, 569.
  • Synthesis of 1,2,3-triazole-linked pyrrolobenzodiazepine conjugates ‘click’ chemistry: DNA-binding affinity and anticancer activity. Kamal, A.; Shankariah, N.; Devaiah, V.; Reddy, K. L.; Juvekar, A. S.;Sen, S.; Kurian, N.; Zingde, S. M.,Bioorg. Med. Chem. Lett.2008, 18, 1468.
  • A facile intramolecular azido/amino reductive cyclization approach: Synthesis of pyrrolobenzodiazepines and their dimers. Kamal, A.; Shankaraiah, N.; Markandeya, N.; Reddy, K. L.; Reddy, Ch. S., Tetrahedron Lett. 2008, 49, 1465.
  • Synthesis, structural characterization and biological evaluation of novel [1,2,4]triazolo[1,5-b][1,2,4]benzothiadiazinebenzothiazole conjugates as potential anticancer agents. Kamal, A.; Khan, M.N.A.; Reddy, K. S.; Srikanth, Y.V.V.; Sridhar, B., Chem. Bio. Drug Design 2008, 71, 78.
  • Base-free monosulfonylation of amines using tosyl or mesylchloride in water. Kamal, A.; Reddy, J. S.; Bharathi, E. V.; Dastagiri, D., Tetrahedron Lett. 2007, 49, 348.
  • Enantioselective synthesis of (R), (S)-curcumene and curcuphenol: An efficient chemoenzymatic route. Kamal, A.; Malik, M. S.; Shaik, A. A.; Azeeza, S., Tetrahedron: Asymm. 2007, 18, 2547.
  • Design, synthesis and biological activity of A-C8/C-C2-linked 6-chloropurine-pyrrolobenzodiazepine hybrids as anticancer agents. Kamal, A.; Shankariah, N.; Reddy, K. L.; Devaiah, V.; Juvekar, A. S.; Sen, S., Letters in Drug Design & Discovery 2007, 4, 596.
  • An efficient synthesis of quinoline derivatives: Bio-active studies. Kamal, A.; Reddy, K. S.; Khan, M.N.A.; Shetti, R.V.C.R.N.C.; Ahmed, S. K.; Kumar K. P.; Murthy, U.S.N., Letters in Drug Design & Discovery 2007, 4, 580.
  • Synthesis and biological evaluation of a new series of benzothiazole-benzothiadiaze conjugates as antibacterial agents. Kamal, A.; Ahmed, S. K.; Reddy, K. S.; Khan, M.N.A.; Shetti, R.V.C.R.N.C.; Siddhardha, B.; Murthy, U.S.N.; Arnab, C.; Nagaraja, V., Letters in Drug Design & Discovery 2007, 4, 550.
  • Synthesis, DNA binding, and cytotoxicity studies of pyrrolo[2,1-c][1,4] benzodiazepine-anthraquinone conjugates. Kamal, A.; Ramu, R.; Tekumalla, V.; Khanna, G. B. R.; Barkume, M. S.; Juvekar, A. S.; Zingde, S. M.,Bioorg. Med. Chem. 2007, 15, 6868.
  • Lipase-catalyzed enantiomer separation of 3-hydroxy-4-(tosyloxy) butanenitrile: Synthesis of (R)-GABOB (3R)-4-amino-3-hydroxybutanoic acid) and (R)-carnitine hydrochloride (2R)-3-carboxy-2-hydroxy-N,N,N-trimethylpropan-1-aminium chloride), Kamal, A.; Khanna, G.B.R.; Krishnaji, T., Helvetica Chimica Acta, 2007, 90, 1723.
  • A new chemoenzymatic Baylis-Hillman approach for the synthesis of enantiomerically enriched umbelactones. Kamal, A.; Krishnaji, T.; Reddy, P. V., Tetrahedron Lett. 2007, 48, 7232.
  • Enantioselective total synthesis of both the stereoisomers of dihydrokawain-5-ol. Kamal, A.; Krishnaji, T.; Reddy, P.V., Tetrahedron: Asymm. 2007, 18, 1775.
  • Sulfamic acid as an efficient and recyclable catalyst for the ring opening of epoxides with amines and anilines: An easy synthesis of b-amino alcohols under solvent free conditions. Kamal, A.; Prasad, B. R.; Reddy, A. M.; Khan, M.N.A., Catalysis Communications 2007, 8, 1876.
  • Copper(II) tetrafluoroborate as a mild and efficient catalyst for the one-pot synthesis  of 3,4-dihydropyrimidin-2(1H)-ones under solvent free conditions. Kamal, A.; Krishnaji, T.; Azhar, M. A., Catalysis Communications 2007, 8, 1929.
  • Anti-tubercular agents. Part IV: Synthesis and antimycobacterial evaluation of nitroheterocyclic based 1,2,4-benzothiadiazines. Kamal, A.; Ahmed, S. K.; Reddy, K. S.; Khan, M.N.A.; Shetti, R.V.C.R.N.C.; Siddardha, B.; Murthy, U.S.N.; Khan, I. A.; Kumar, M.; Sharma, S.; Ram, A. B., Bioorg. Med. Chem. Lett. 2007, 17, 5419.
  • Synthesis, structure analysis, and antibacterial activity of some novel 10-substituted 2-(4-piperidyl/phenyl)-5-5-dioxo[1,2,4]triazolo[1,5-b][1,2,4] benzothiadiazine derivatives. Kamal, A.; Khan, M.N.A.; Reddy, K. S.; Rohini, K.; Sastry,G. N.; Sateesh, B.; Sridhar,B., Bioorg. Med. Chem. Lett., 2007, 17, 5400.
  • 1,2,4-Benzothiadiazine linked pyrrolo[2,1-c][1,4]benzodiazepine conjugates: Synthesis, DNA-binding affinity and cytotoxicity. Kamal, A.; Khan, M.N.A.; Reddy, K. S.; Ahmed, S. K.; Kumar, M. S.; Juvekar, A. S.; Sen, S.; Zingde, S. M., Bioorg. Med. Chem. Lett. 2007, 17, 5345.
  • TMSCI-Nal-mediated reaction of aryl azides with cyclic enol ethers: An efficient one-pot synthesis of 1,2,3,4-tetrahydroquinolines. Kamal, A.; Prasad, B. R.; Khan, M.N.A.; J. Mol. Cat. A: Chemical 2007,274, 133.
  • Direct one-pot synthesis of b-hydroxysulfides from terminal olefins in a mixture of [bmim][BF4] and water in presence of molecular oxygen. Kamal, A.; Reddy, D.R.S.; Rajender, J. Mol. Cat. A: Chemical 2007, 272, 26.
  • Lipase-catalyzed resolution of N-(3-cyano-2-hydroxy propan-1-yl)phthalimide synthesis of (R)-GABOB and (R)-carnitine. Kamal, A.; Krishnaji, T.; Khan, M.N.A., J. Mol. Cat. B: Enzymatic 2007, 47, 1.
  • Al(OTf)3 as a highly efficient catalyst for the rapid acetylation of alcohols, phenols and thiophenols under solvent-free conditions. Kamal, A.; Khan, M.N.A.; Reddy, K. S.; Srikanth, Y.V.V.; Krishnaji, T., Tetrahedron Lett. 2007, 48, 3813.
  • Efficient solid-phase synthesis of a library of imidazo[1,2-a]pyridine-8-carboxamides. Kamal, A.; Devaiah, V.; Reddy, K. L.; Rajender; Shetti, R.V.C.R.N.C.; Shankaraiah, N., J. Comb. Chem. 2007, 9, 267.
  • Synthesis and DNA-binding ability of C2R-fluoro substituted DC-81 and its dimers. Kamal, A.; Reddy, D.R.S.; Reddy, P.S.M.M., Bioorg. Med. Chem. Lett.2007, 17, 803.
  • Solid-phase synthesis of a library of pyrrolo[2,1-c][1,4]benzodiazepin-5,11-diones with potential antitubercular activity. Kamal, A.; Reddy, K. L.; Devaiah, V.; Shankaraiah, N.; Reddy, G.S.K.; Raghavan, S., J. Comb. Chem. 2007, 9, 29.
  • Synthesis of a new class of 2-anilino substituted nicotinyl arylsulfonyl hydrazides as potential anticancer and antibacterial agents. Kamal, A.; Khan, M.N.A.; Reddy, K. S.; Rohini, K., Bioorg. Med. Chem. 2007, 15, 1004.
  • Chemoenzymatic synthesis of (5S) and (5R)-hydroxymethyl-3,5-dimethyl-4-(methoxymethoxy)-5H-thiophen-2-one: A precursor of thiolactomycin and determination of its absolute configuration, Kamal, A.; Shaik, A. A.; Azeeza, S.; Malik, M. S.; Sandbhor, M., Tetrahedron: Asymm. 2006, 17, 2890.
  • Chemoenzymatic synthesis of (3R,4S)- and (3S,4R)-3-methoxy-4-methylaminopyrrolidine. Kamal, A.; Shaik, A. A.; Sandbhor, M.; Malik, M. S.; Azeeza, S., Tetrahedron: Asymm. 2006, 17, 2876.
  • Chemoenzymatic synthesis of enantiomerically enriched kavalactones. Kamal, A.; Krishnaji, T.; Khanna, G.B.R., Tetrahedron Lett. 2006, 47, 8657.
  • An efficient solid-phase synthesis of biologically important DNA-interactive pyrrolo[2,1-c][1,4]benzodiazepine dimers (DSB-120) and their C2-fluorinated analogues. Kamal, A.; Shankaraiah, N.; Devaiah, V.; Reddy, K. L., Tetrahedron Lett. 2006, 47, 6553.
  • Synthesis and biological evaluation of coumarin linked fluoroquinolones phthalimides and naphthalimides as potential DNA-gyrase inhibitors. Kamal, A.; Satyanarayana, M.; Devaiah, V.; Rohini, V.; Yadav, J. S.; Bullick, B.; Nagaraja, V.,Letters in Drug Design & Discovery 2006, 3, 494.
  • Lipase-mediate resolution of 3-hydroxy-4-trityloxybutanenitrile: Synthesis of 2-amino alcohols, oxazolidinones and GABOB. Kamal, A.; Khanna, G.B.R.; Krishnaji, T.; Ramu, R., Tetrahedron: Asymm. 2006, 17, 1281.
  • Solid-phase synthesis of fused [2,1-b] quinazolinone alkaloids. Kamal, A.; Shankaraiah, N.; Devaiah, V.; Reddy, K. L., Tetrahedron Lett. 2006, 47, 9025.
  • Selective reduction of aromatic azides in solution/solid-phase and resin cleavage by employing BF3. OEt2/EtSH. Preparation of DC-81. Kamal, A.; Shankaraiah, N.; Reddy, K. L.; Devaiah, V., Tetrahedron Lett. 2006, 47, 4253.
  • Synthesis and biological activity of new 4b-N-heteroaryl analogues of podophyllotoxin. Kamal, A.; Kumar,B. A.; Arifuddin,M.; Dastidar,S.G., Letters in Drug Design & Discovery 2006, 3, 205.
  • Polyethylene glycol (PEG) as an efficient recyclable medium for the synthesis of b-amino sulfides. Kamal, A; Reddy, D.R.S.;Rajender, Tetrahedron Lett. 2006, 47, 2261.
  • Synthesis and DNA-binding ability of pyrrolo[2,1-c][1,4]benzodiazepine-azepane conjugates. Kamal, A; Reddy, D. R.S.; Reddy, P.S.M.M.; Rajender,Bioorg. Med. Chem. Lett., 2006, 16, 1160.
  • Conversion of amines to imines employing polymer-supported sulfoxide (PSS) and polymer-supported perruthenate (PSP): Synthesis of pyrrolo[2,1-c][1,4]benzodiazepines. Kamal, A.; Devaiah, V.; Reddy, K. L.; Shankaraiah, N., Adv. Syn. Cat. 2006, 348, 249.
  • DNA binding potential and cytotoxicity of newly designed pyrrolobenzodiazepine dimers linked through a piperazine side-armed-alkane spacer. Kamal, A; Reddy, P.S.M.M.; Reddy, D.R.S.; Laxman, E., Bioorg. Med. Chem. 2006, 14, 385.
  • Anti-tubercular agents. Part 3: Benzothiadiazine as a novel scaffold for anti-Mycobacterium activity. Kamal, A.; Reddy, K. S.; Ahmed, S. K.; Khan, M.N.A.; Sinha, R. K.; Yadav, J. S.; Arora, S. K., Bioorg. Med. Chem. 2006, 14, 650.
  • Recent advances in the solid-phase combinatorial synthetic strategies for the benzodiazepine based privileged structures. Kamal, A.; Reddy, K. L.; Devaiah, V.; Shankaraiah, N.; Reddy, D.R.S., Mini-Reviews in Medicinal Chemistry 2006, 6, 53.
  • Recent advances in the solid-phase combinatorial synthetic strategies for the quinoxaline, quninazoline and benzimidazole based privileged structures. Kamal, A.; Reddy, K. L.; Devaiah, V.; Shankaraiah, N.; Rao, M. V.; Mini-Reviews in Medicinal Chemistry 2006, 6, 70.
  • A polymer-assisted solution-phase strategy for the synthesis of fused [2,1-b] quinazolinones and the preparation of optically active l-vasicinone. Kamal, A.; Devaiah, V.; Shankaraiah, N.; Reddy, K. L., Synlett 2006, 16, 2609.
  • Chemoenzymatic synthesis of calcilytic agent NPS-2143 employing a lipase-mediated resolution protocol. Kamal, A.; Chouhan, G., Tetrahedron: Asymm. 2005, 16, 2784.
  • A simple and green procedure for the conjugate addition of thiols to conjugated alkenes employing polyethylene glycol (PEG) as an efficient recyclable medium. Kamal, A.; Reddy, D.R.S.; Rajender, Tetrahedron Lett. 2005, 46, 7951.
  • Synthesis and biological evaluation of new 4β-anilino and 4β-imido substituted podophyllotoxin congeners. Kamal, A; Gayatri, N. L.; Reddy, D.R.S.; Reddy, P.S.M.M.; Arifuddin, M.; Dastidar, S. G.; Kondapi, A. K.; Rajkumar, M., Bioorg. Med. Chem. 2005, 13, 6218.
  • Bi(OTf3) – catalyzed regioselective ring opening of epoxides with phenols; facile synthesis of 1,3-diaryloxy-2-propanols. Kamal, A.; Ahmed, S. K.; Sandbhor, M.; Khan, M.N.A.; Arifuddin, M., Chemistry Lett. 2005, 34, 1142.
  • A facile and convenient chemoenzymatic synthesis of optically active O-(4-methoxy phenyl)-glycidol and 1,2-diacyl-sn-glycerol. Kamal, A.; Sandbhor, M.; Shaik, A. A.; Malik, M. S., Tetrahedron: Asymm. 2005, 16, 1855.
  • Synthesis of pyrrolo[2,1-c][1,4] benzodiazepines and their conjugates by azido reductive cyclization strategy as potential DNA binding agents. Kamal, A.; Hariabu,A.; Ramana, A. V.; Ramana,K. V.; Bharathi, E. V.; Kumar, M. S.,  Bioorg. Med. Chem. Lett. 2005, 15, 2621.
  • Copper(II) tetrafluoroborate-catalyzed ring-opening of epoxides by amines. Kamal, A.; Ramu, R.; Aziz, M. A.; Khanna, G.B.R., Tetrahedron Lett. 2005, 15, 2675.
  • New chemoenzymatic pathway for b-adrenergic blocking agents. Kamal, A.; Khanna, G.B.R.; Krishnaji, T.; Venkatesh, T.; Ramu, R., Tetrahedron: Asymm. 2005, 16, 1485.
  • Antitubercular agents. Part 2: New thiolactomycin analogues active against Mycobacterium tuberculosis. Kamal, A.; Shaik,A. A.; Sinha,R.; Yadav, J. S.; Arora,S. K., Bioorg. Med. Chem. Lett. 2005, 15, 1927.
  • Antitubercular agents. Part 1: Synthesis of phthalimido- and naphthalimido- linked phenazines as new prototype antitubercular agents. Kamal, A.; Haribabu, A.; Ramana, A. V.; Sinha, R.; Yadav, J. S.; Arora, S. K., Bioorg. Med. Chem. Lett., 2005, 15, 1923.
  • Ultrasonic activated efficient method for the cleavage of epoxides with aromatic amines. Kamal, A.; Adfil, S. F.; Arifuddin, M., Ultrasonics Sonochemistry 2005, 12, 429.
  • A task-specific ionic liquid [bmim]SCN for the conversion of alkyl halides to alkyl thiocyanates at room temperature. Kamal, A.; Chouhan, G., Tetrahedron Lett. 2005, 46, 1489.
  • Synthesis and evaluation of new pyrrolo[2,1-c][1,4]benzodiazepine hybrids linked to a flavone moiety. Kamal, A.; Ramu, R.; Khanna, G.B.R.; Saxena, A. K.; Shanmugavel, M.; Pandita, R. M., Arkivoc 2005, 83.
  • A new facile chemoenzymatic synthesis of levamisole. Kamal, A.; Khanna, G.B.R.; Krishnaji, T.; Ramu, R., Bioorg.  Med. Chem. Lett. 2005, 15, 613.
  • Synthesis and biological activity of fluoroquinolone-pyrrolo[2,1-c][1,4] benzodiazepine conjugates. Kamal, A.; Devaiah, V.; Reddy, K. L.; Kumar, M. S., Bioorg. Med. Chem., 2005, 13, 2021.
  • Synthesis and biological activity of C-8 fluoroaryl substituted pyrimidine linked pyrrolobenzodiazepine conjugates. Kamal, A.; Reddy, K. L.; Devaiah, V.; Shankaraiah, N.; Kumar, M. S.; Reddy, G. K., Letters in Drug Design & Discovery, 2005, 2, 55.
  • Chemoenzymatic synthesis of (R)- and (S)-tembamide, aegeline and denopamine by a one-pot lipase resolution protocol. Kamal, A.; Shaik, A. A.; Sandbhor, M.; Malik, M. S., Tetrahedron: Asymm 2004, 15, 3939.
  • Chemoenzymatic synthesis of enantiomerically pure 1,2-diols by employing immobilized lipase in the ionic liquid [bmim]PF6, Kamal, A.; Chouhan, G., Tetrahedron Lett. 2004, 45, 8801.
  • Synthesis of DNA-interactive pyrrolo[2,1-c][1,4]benzodiazepines by employing polymer supported reagents: Preparation of DC-81,Kamal, A.; Reddy, K. L.; Devaiah, V.; Shankaraiah, N., Synlett 2004, 14, 2533.
  • Design, synthesis, and evaluation of mixed imine-amine pyrrolobenzodiazepine dimers with efficient DNA binding affinity and potent cytotoxicity, Kamal, A.; Ramesh, G.; Srinivas, O.; Ramulu, P.; Laxman, N.; Rahena, T.; Deepak, M.; Achary, M. S.; Nagarajaram, H. A., Bioorg. Med. Chem. 2004, 12, 5427.
  • Synthesis of fluorinated analogues of SJG-136 and their DNA-binding potential, Kamal, A.; Reddy, P.S.M.M.; Reddy, D.R.S.; Laxman, E.; Murthy, Y.L.N., Bioorg. Med. Chem. Lett. 2004, 14, 5699.
  • One pot conversion of azido arenes to N-arylacetamides and N-arylformamides: Synthesis of 1,4-benzodiazepine-2,5-diones and fused [2,1-b]quinazolinones, Kamal, A.; Ramana, A.V.; Reddy, K. S.; Ramana, K.V.; Haribabu, A.; Prasad, B. R., Tetrahedron Lett. 2004, 45, 8187.
  • Chemoenzymatic synthesis of (3S, 4S)- and (3R,4R)-3-methoxy-4-methylamino-pyrrolidine, Kamal, A.; Shaik,A. A.; Sandbhor, M.; Malik, M. S.; Kaga, H., Tetrahedron Lett. 2004, 45, 8057.
  • A new approach for the solid-phase synthesis of pyrrolo[2,1-c][1,4] benzodiazepines involving reductive cleavage, Kamal, A.; Reddy, K. L.; Devaiah, V.; Shankaraiah, N.; Reddy, Y. N., Tetrahedron Lett. 2004, 45, 7667.
  • Pyrrolo[2,1-c][1,4]benzodiazepine-anthraquinoneconjugates :  Synthesis, DNA-binding and cytotoxicity, Kamal, A.; Ramu, R.; Khanna, G.B.R.; Saxena, A. K.; Shanmugavel, M.; Pandita, R. M., Bioorg. Med. Chem. Lett. 2004, 14, 4907.
  • Synthesis of C-8-linked pyrrolo[2,1-c][1,4] benzodiazepine-benzimidazole conjugates with remarkable DNA-binding affinity, Kamal, A.; Ramulu, P.; Srinivas, O.; Ramesh, G.; Kumar, P.P., Bioorg. Med. Chem. Lett. 2004, 14, 4791.
  • Synthesis and DNA binding affinity of novel A-C8/C-C2-exo unsaturated alkoxyamido-linked pyrrolo[2,1-c][1,4]benzodiazepine dimers, Kamal, A.; Srinivas, O.; Ramulu, P.; Kumar, P. P.; Ramesh, G.; Kumar, M. S., Bioorg. Med. Chem. 2004, 12, 4337.
  • Design, synthesis, biological evaluation and QSAR studies of novel bisepipodophyllotoxins as cytotoxic agents, Kamal, A.; Laxman, E.; Khanna, G.B.R.; Reddy, P.S.M.M.; Rehana, T.; Arifuddin, M.; Neelima, K.; Kondapi, A. K.; Dastidar, S. G., Bioorg. Med. Chem. 2004, 12, 4197.
  • Microwave enhanced reduction of nitro and azido arenes to N-arylformamides employing Zn-HCO2NH4 system: Synthesis of 4(3H)-quinazolinones and pyrrolo[2,1-c][1,4]benzodiazepines, Kamal, A.; Reddy, K. S.; Prasad, B. R.; Haribabu, A.; Ramana, A. V., Tetrahedron Lett. 2004, 45, 6517.
  • Chemoenzymatic synthesis of (S) and (R)-propranolol and sotalol employing one-pot lipase resolution protocol, Kamal, A.; Sandbhor, M.; Shaik, A. A., Bioorg. Med. Chem. Lett.2004, 14, 4581.
  • Facile and efficient solid-phase synthesis of DNA-interactive pyrrolo[2,1-c][1,4]benzodiazepines, Kamal, A.; Reddy, K. L.; Devaiah, V.; Shankaraiah, N., Synlett. 2004, 1841.
  • Synthesis of C8-linked pyrrolo[2,1-c][1,4]benzodiazepine-acridone/acridine hybrids as potential DNA-binding agents, Kamal, A.; Srinivas, O, ; Ramulu, P.; Ramesh, G.; Kumar, P. P., Bioorg. Med. Chem. Lett., 2004, 14, 4107.
  • The effect of C2-fluoro group on the biological activity of DC-81 and its Dimers, Kamal, A.; Reddy, P.S.M.M.; Reddy, D.R.S., Bioorg. Med. Chem. Lett.2004, 14, 2669.
  • Investigation towards the chemoselective thioacetalization of carbonyl compounds by using ionic liquid [brim]Br as a recyclable catalytic medium, Kamal, A.; Chouhan, G., Adv. Synth. Cat. 2004, 346, 579.
  • Selective reduction of aromatic azides with hexamethyldisilathiane: Synthesis of new 2-azidopyrrolo[2,1-c][1,4]benzodiazepines, Kamal, A.; Reddy, K. L.; Reddy, G.S.K.; Reddy, B.S.N., Tetrahedron Lett. 2004, 45, 3499.
  • FeCl3-NaI mediated reactions of aryl azides with 3,4-dihydro-2H-pyran: A convenient synthesis of pyranoquinolines, Kamal, A.; Prasad, B. R.; Ramana, A. V.; Haribabu, A.; Reddy, K. S., Tetrahedron Lett. 2004, 45, 3507.
  • Synthesis of enantiopure b-azidoalcohols from their ketoazides by reduction with NaBH4 in the presence of alumina and in situ lipase resolution, Kamal, A.; Shaik, A. A.; Sandbhor, M.; Malik, M. S., Tetrahedron: Asymm.2004, 15, 935.
  • Synthesis and antitumour activity of pyrene-linked pyrrolo[2,1-c][1,4] benzodiazepine hybrids, Kamal, A.; Ramesh, G.; Srinivas, O.; Ramulu, P., Bioorg. Med. Chem. Lett. 2004, 14, 471.
  • An efficient and facile nitration of phenols with nitric acid / zinc chloride under ultrasonic conditions, Kamal, A.; Kumar, B. A.; Arifuddin, M.; Patrick, M., Ultrasonics Sonochemistry 2004, 11, 455. 
  • Chemoenzymatic synthesis of enantiomerically pure terminal 1,2-diols, Kamal, A.; Sandbhor, M.; Ahmed, S. K.; Adil, S. F.; Shaik, A. A., Tetrahedron: Asymm.2003, 14, 3861.
  • Synthesis and DNA-binding affinity of A-C8/C-C2 alkoxyamido-linked pyrrolo[2,1-c][1,4]benzodiazepine dimers, Kamal, A.; Ramulu, P.; Srinivas, O.; Ramesh, G., Bioorg. Med. Chem. Lett. 2003, 13, 3955.
  • A One-Pot, efficient and facile synthesis of 4b-arylaminopodophyllotoxins: Synthesis of NPF and GL-331 as DNA topoisomerase II Inhibitors, Kamal, A.; Kumar, B. A.; Arifuddin, M., Tetrahedron Lett. 2003, 44, 8457. 
  • Synthesis of 4b-amido and 4b-sulphonamidoanalogues of podophyllotoxin as potential antitumour agents, Kamal, A.; Kumar, B. A.; Arifuddin, M.; Dastidar, S. G., Bioorg. Med. Chem. 2003, 11, 5135. 
  • One-pot synthesis and resolution of chiral allylic alcohols, Kamal, A.; Sandbhor, M.; Shaik, A. A.; Sravanthi, V., Tetrahedron: Asymm.2003, 14, 2839.
  • Synthesis of novel C2 and C2-C8 linked pyrrolo[2,1-c][1,4]benzodiazepine-naphthalimide hybrids as DNA-binding agents, Kamal, A.; Srinivas, O.; Ramulu, P.; Ramesh, G.; P. P. Kumar., Bioorg. Med. Chem. Lett. 2003, 13, 3577. 
  • Synthesis of C-8 methanesulphonate substituted pyrrolobenzodiazepines as potential antitumour agents, Kamal, A.; Ramulu, P.; Srinivas, O.; Ramesh, G., Bioorg. Med. Chem. Lett. 2003, 13, 3517.
  • Design and synthesis of novel chrysene-linked Pyrrolo[2,1-c][1,4]-benzodiazepine hybrids as potential DNA-binding agents, Kamal, A.; Ramesh, G.; Ramulu, P.; Srinivas, O.; Rehana, T.; Sheelu, G., Bioorg. Med. Chem. Lett. 2003, 13, 3451.
  • Chemoenzymatic enantioselective synthesis of 3-hydroxy-2-pyrrolidinones and 3-hydroxy-2-piperidinones, Kamal, A.; Ramana, K. V.; Ramana, A. V.; Haribabu, A., Tetrahedron: Asymm. 2003, 14, 2587.
  • Chemoenzymatic synthesis of duloxetine and its enantiomer: Lipase catalyzed resolution of 3-hydroxy-3-(2-thienyl) propanenitrile, Kamal, A.; Khanna, G.B.R.; Ramu, R.; Krishnaji, T., Tetrahedron Lett. 2003, 44, 4783.
  • Facile reduction of aromatic nitro/azido functionality on solid support employing Al-NiCl2.6H2O and Al/NH4Cl: Synthesis of pyrrolo[2,1-c][1,4]benzodiazepines, Kamal, A.;Reddy, K. L.; Devaiah, V.; Reddy, G.S.K., Tetrahedron Lett. 2003, 44, 4741.
  • Application of one-pot lipase resolution strategy for the synthesis of chiral g- and d- lactones, Kamal, A.; Sandbhor, M.; Shaik, A. A., Tetrahedron: Assymetry, 2003, 14, 1575. 
  • Chemoselective thioacetalization and transthioacetalization of carbonyl compounds catalyzed by immobilized ccandium (III) triflate in ionic liquids, Kamal, A.; Chouhan, G., Tetrahedron Lett. 2003, 44, 3337.
  • An efficient catalytic deprotection of thioacetals employing bismuth triflate: Synthesis of pyrrolo[2,1-c][1,4]benzodiazepines, Kamal, A.; Reddy, P.S.M.M.; Reddy, D.R.S., Tetrahedron Lett. 2003, 44, 2857.
  • Chemoenzymatic synthesis of both enantiomers of fluoxetine, tomoxetine and nisoxetine: Lipase catalyzed resolution of 3-aryl-3-hydroxy propanenitrile, Kamal, A.; Khanna, G.B.R.; Ramu, R., Tetrahedron: Asymm. 2002, 13, 2039.
  • Design, synthesis, and evaluation of new non-cross-linking pyrrolobenzodiazepine dimers with efficient DNA binding ability and potent antitumor activity, Kamal, A.; Ramesh, G.; Laxman, N.; Ramulu, P.; Srinivas, O.; Neelima, K.; Kondapi, A. K.; Sreenu, V.B.; Nagarajaram, H. A., J. Med. Chem. 2002, 45, 4679.
  • Facile and efficient synthesis of fluoroalkyl aryl ethers, Kamal, A.; Ramana, K. V.; Ramana, A. V.; Haribabu, A., Tetrahedron Lett. 2002, 43, 7353.
  • Mild and efficient reduction of azides to amines: Synthesis of fused [2,1-b] quinazolinones, Kamal, A.; Ramana, K. V.; Haribabu, A.; Ramana, A. V., Tetrahedron Lett. 2002, 43, 6861.
  • Simple and facile reduction of azides to amines: Synthesis of DNA interactive pyrrolo[2,1-c][1,4]benzodiazepines, Kamal, A.; Reddy, P.S.M.M.; Reddy, D.R.S., Tetrahedron Lett. 2002, 43, 6629.
  • Design and synthesis of C-8 linked pyrrolo benzodiazepine-napthalimide hybrids as anticancer agents, Kamal, A.; Reddy, B.S.N.; Reddy, G.S.K.; Ramesh, G., Bioorg. Med. Chem. Lett., 2002, 12, 1933. 
  • Synthesis of C8-alkylamino substituted pyrrolo[2,1-c][1,4]benzodiazepines as potential anticancer agents, Kamal, A.; Laxman, N.; Ramesh, G.; Srinivas, O.; Ramulu, P., Bioorg, Med. Chem. Lett.2002, 12, 1917.
  • One-pot lipase-catalyzed synthesis of enantiopure secondary alcohols from carbonyl compounds: A new protocol for lipase-mediated resolution, Kamal, A.; Sandbhor, M.; Ramana, K. V., Tetrahedron: Asymm. 2002, 13, 815.
  • Efficient chemoenzymatic synthesis of (S) and (R)-5-(1-aminoethyl)-2- (cyclohexylmethoxy)benzamide: Key intermediate for Src-SH2inhibitor, Kamal, A.; Sandbhor, M., Bioorg. Med. Chem. Lett. 2002, 12, 1735.
  • Oxathiacetalization, thioacetalization and transthioacetalization of carbonyl compounds by N- bromosuccinimide: Selectivity and scope, Kamal, A.; Chouhan, G.; Ahmed, K., Tetrahedron Lett. 2002, 43, 6947.
  • Recent developments in the design, synthesis and structure activity relationship studies of pyrrolo[2,1-c][1,4]benzodiazepines as DNA-interactive antitumor antibiotics, Kamal, A.; Rao, M. V.; Laxman, N.; Ramesh, G.; Reddy, G.S.K., Curr. Med. Chem. Anti-Cancer Agents 2002, 2, 215.
  • Efficient solid phase synthesis of DNA-interactive pyrrolo[2,1-c][1,4] benzodiazepine antitumour antibiotics, Kamal, A.; Reddy, G.S.K.; Reddy, K. L.; Raghavan, S., Tetrahedron Lett. 2002, 43, 2103.
  • Scandium triflate as a recyclable catalyst for chemoselective thioacetalization, Kamal, A.; Chouhan, G., Tetrahedron Lett. 2002, 43, 1347.
  • Mild and efficient chemoselective protection of aldehydes as dithioacetals employing N-bromosuccinimide, Kamal, A.; Chouhan, G., Synlett, 2002, 474. 
  • Efficient reduction of aromatic nitro/azido groups on solid support Employing indium: Synthesis of pyrrolo[2,1-c][1,4]benzodiazepine-5,11-Diones, Kamal, A.; Reddy, G.S.K.; Reddy, K. L., Tetrahedron Lett. 2001, 42, 6969.
  • Enzymatic resolution of b-hydroxy nitriles employing lipases, Kamal, A.; Khanna, G.B.R., Tetrahedron: Asymm. 2001, 12, 405.
  • Chemoenzymatic synthesis of pyrrolo[2,1-b]quinazolinone: Lipase catalyzed resolution of vasicinones, Kamal, A.; Ramana, K. V.; Rao, M. V., J. Org. Chem. 2001, 66, 997.
  • Synthesis of novel non-cross linking pyrrolobenzodiazepines with remarkable DNA-binding affinity and potent antitumour activity, Kamal, A.; Laxman, N.; Ramesh, G.; Neelima, K.; Kumar, K. A., Chem. Commun. 2001, 437.
  • Solid phase synthesis of pyrrolo[2,1-c][1,4]benzodiazepine 5,11-diones, Kamal, A.; Reddy, G.S.K.; Raghavan, S., Bioorg. Med. Chem. Lett. 2001, 11, 387. 
  • New halogenation reagent system for one-pot conversion of alcohols to iodides, Kamal, A.; Ramesh, G.; Laxman, N., Synth. Commun. 2001, 31, 29.
  • Reductive cyclization of w-azido/nitro carbonyl compounds by samarium iodide: A facile preparation of DNA-binding pyrrolo[2,1-c][1,4]benzodiazepine and its Dimers, Kamal, A.; Laxman, E.; Reddy, P.S.M.M., Tetrahedron Lett. 2000, 41, 8631.
  • A facile and rapid regeneration of carbonyl compounds from their N,N-dimethylhydrazones employing transition metal complexes, Kamal, A.; Arifuddin, M.; Rao, M. V., Synlett 2000, 1482.
  • Synthesis of pyrrolo[2,1-c][1,4]benzodiazepine via reductive cyclization of w-azido carbonyl compounds by TMSI: An efficient preparation of antibiotic DC-81 and its dimers, Kamal, A.; Laxman, E.; Laxman, N.; Rao, N. V., Bioorg. Med. Chem. Lett, 2000, 2311.
  • A mild and efficient dethioacetalization employing FeCl3.6H2O: DNA-binding Pyrrolo[2,1-c][1,4]benzodiazepine ring system and its dimers, Kamal, A.; Laxman, E.; Reddy, P.S.M.M., Synlett 2000, 1476. 
  • An efficient reduction of azides to amines: Synthesis of DNA interactive pyrrolo[2,1-c][1,4]benzodiazepines, Kamal, A.; Laxman, E.; Arifuddin, M., Tetrahedron Lett. 2000, 41, 7743.
  • Facile and efficient one-pot synthesis of 4b-arylaminopodophylotoxins: Synthesis of DNA-topoisomerase II inhibitors (NPF and W-68), Kamal, A.; Laxman, N.; Ramesh, G., Bioorg. Med. Chem. Lett. 2000, 10, 2059.
  • Crystal structure of picropodophyllin, Kamal, A.; Chandramohan, K.; Kumar, K. R.; Damayanthi, Y., Z. Kristallogr. 2000, 45, 215.
  • Enantioselective ring opening of epoxides with trimethylsilyl azide (TMSN3) in the presence of b-cyclodextrin: An efficient route to 1,2-azido alcohols, Kamal, A.; Arifuddin, M.; Rao, M.V., Tetrahedron Asymm. 1999, 10, 4261.
  • Microwave assisted synthesis of pyrrolo-[2,1-c][1,4] benzodiazepine-5,11-diones, Kamal, A.; Reddy, B.S.N.; Reddy, G.S.K., Synlett 1999, 1251.
  • A mild and rapid regeneration of alcohols from their allylic ethers by chlorotrimethylsilane/sodium iodide, Laxman, E.; Rao, N.V., Tetrahedron Lett. 1999, 40, 371.
  • An efficient and rapid regeneration of carbonyl compounds from their N,N-dimethylhydrazones by chloromethyl-silane/sodium iodide, Kamal, A.; Ramana, K.V.; Arifuddin, M., Chemistry Lett. 1999, 827.
  • The newer synthetic strategies for DNA binding pyrrolobenzodiazepine antibiotics, Kamal, A.; Rao, M.V.; Reddy, B.S.N., Chemistry of Heterocyclic Compounds 1998, 12, 1588.
  • Facile and improved synthesis of 4b-aminopodophyllotoxin congeners, Kamal, A.; Gayatri, N.L.; Rao, N. V., Bioorg. Med. Chem. Lett. 1998, 8, 3097. 
  • Efficient one-pot synthesis of N-substituted phthalimides/ naphthalimides from azides and anhydrides by idotrimethylsilane, Kamal, A.; Laxman, E.; Laxman, N.; Rao, N.V., Tetrahedron Lett. 1998, 39, 8733.
  • Improved efficient conversion of aldehydes to nitriles via their N,N-dimethylhydrazones, Kamal, A.; Arifuddin, M.; Rao, N. V., Synth. Commun. 1998, 28, 4507. 
  • Facile transformation of N,N-dimethylhydrazones to ketones with dimethylsulphate and potassium carbonate, Kamal, A.; Arifuddin, M.; Rao, N.V., Synth. Commun. 1998, 28, 3927. 
  • A mild and facile reduction of azides to the amines by N,N-dimethylhydrazine and catalytic ferric chloride, Kamal, A.; Reddy, B.S.N., Chemistry Lett. 1998, 593.
  • Iodotrimethylsilane: A mild and efficient reagent for the reduction of azides to amines, Kamal, A.; Rao, N.V.; Laxman, E., Tetrahedron Lett. 1997, 38, 6945.
  • An efficient synthesis of pyrrolo[2,1-c][1,4]benzodiazepine antibiotics via reductive cyclization, Kamal, A.; Reddy, B.S.N.; Reddy, B.S.P., Bioorg. Med. Chem. Lett. 1997, 7, 1825.
  • Stereo and chemoselective enzymatic reduction azido functionality: Synthesis of 4b-aminopodophyllotoxin congeners by Baker’s Yeast, Kamal, A.; Laxminarayana, A.; Gayatri, N. L., Tetrahedron Lett.1997, 38, 6871.
  • A novel dehydrogenation of podopyllotoxin by Yeast cells, Kamal, A.; Damayanthi, Y., Bioorg. Med. Chem. Lett. 1997, 7, 657.
  • Novel biocatalytic reduction of aryl azides: Chemo-enzymatic synthesis of pyrrolo[2,1-c][1,4]benzodiazepine antibiotics, Kamal, A.; Damayanthi, Y.; Reddy, B.S.N.; Laxminarayana, B.; Reddy, B.S.P., Chem. Commun. 1997, 1015.
  • Synthesis of Pyrrolo[2,1-c][1,4]benzodiazepine antibiotics: Oxidation of cyclic secondary amine with TPAP, Kamal, A.; Howard, P.; Reddy, B.S.N.; Reddy, B.S.P.; Thurston, D. E., Tetrahedron 1997, 53, 3223.
  • Synthesis of pyrrolo[2,1-c][1,4]benzodiazepine antibiotics: via azido reductive cyclization with HMDST, Kamal, A.; Reddy, B.S.P.; Reddy, B.S.N., Tetrahedron Lett.1996, 37, 6803.
  • Mass spectral study of etoposide, Vairamini, M.; Suma, K.; Kamal, A.; Gayatri, N. L., Rapid Commun. Mass Spectrom.1996, 10, 817.
  • An efficient method for 4b-anilino-4-demethylepi-podophyllotoxin synthesis of NPF and W-68, Kamal, A.; Gayatri, N. L., Tetrahedron Lett. 1996, 37, 3359.
  • A new facile procedure for the preparation of pyrrolo[2,1-c][1,4]benzodiazepines: Synthesis of the antibiotics DC-81 and its thio analogues, Kamal, A.; Reddy, B.S.P.; Reddy, B.S.N., Tetrahedon Lett. 1996, 37, 2281.
  • A new route for the synthesis of pyrrolo[2,1-c][1,4]benzodiazepine antibiotics via oxidation of cyclic secondary amine , Kamal, A.; Rao, M. V., Chem. Commun. 1996, 385.
  • Syntheis of podophyllotoxin congeners as potential DNA topoisomerase II inhibitor, Kamal, A.; Atchison, K.; Daneshtalab, M.; Micetich, R. G., Anticancer Drug Design 1995, 10, 545. 
  • Facile and efficient synthesis of the dimers of DC-81 antitumor antibiotics, Kamal, A.; Rao, M. V., Tetrahedron Lett. 1995, 36, 4299. 
  • A rapid entry into podophyllotoxin congeners; Synthesis of justicidin B, Kamal, A.; Daneshtalab, M.; Micetich, R. G., Tetrahedron Lett. 1994, 35, 3879. 
  • Enzyme catalyzed stereoselective synthesis of (S)-propranolamines, Kamal, A.; Rao, M. V., Tetrahedron Asymmetry 1994, 5, 1881.
  • Synthesis of ring A-opened isopicropodophyllins as potential DNA topoisomerase II inhibitors, M. Daneshtalab, Kamal, A.; Atchison, K.; Micetich, R. G., Bioorg. Med. Chem. Lett. 1994, 4, 1513. 
  • Synthesis and antimicrobial activity of 5-thioabbeymycin: Limitations of the iminothio ether approach to carbinolamine containing pyrrolobenzo-diazepines, Kamal, A.; Reddy, B.S.P.; Thurston, D. E., Bioorg. Med. Chem. Lett. 1993, 3, 743.
  • Stereoselective synthesis of (S)-propanolamines lipase catalyzed opening of epoxides with 2-propylamine, Kamal, A.; Damayanthi, Y.; Rao, M.V., Tetrahedron Asymm. 1992, 3, 1361. 
  • Enzymatic regeneration of aldehydes and ketones from hydrazones and oximes by Baker’s Yeast in organic solvents, Kamal, A.; Reddy, B.S.P., Biotech. Lett. 1992, 14, 929. 
  • Stereoselective synthesis of (S)-propanol amines: Liver microsomes mediated opening of epoxides with arylamines, Kamal, A.; Rao, A. B.; Rao, M.V., Tetrahedron Lett.1992, 33, 4077.
  • Enzymatic deoximation of oximes by ultrasonically stimulated Baker’s Yeast, Kamal, A.; Rao, M.V.; Meshram, H. M., J. Chem. Soc. Perkin Trans. 1991, 1, 2056.
  • Lipase-catalyzed resolution: enantioelective esterfication of 2-propanolamines, Kamal, A.; Rao, M.V., Tetrahedron Assymetry 1991, 2, 751.
  • Enzymatic regiospecific oxidative conversion of 5-thio to 5-oxo by Baker’s yeast in 5, 11-dithiopyrrolo[1,4] benzodiazepine antibiotics, Kamal, A.; Reddy, B. S. P., Bioorg. Med. Chem. Lett. 1991, 1, 159. 
  • Efficient enzymatic hydrazone hydrolysis by Baker’s Yeast, Kamal, A.; Rao, M.V.; Meshram, H. M., Tetrahedron Lett. 1991, 32, 2657. 
  • Stereoselective metabolism of 3-isopropyl-5-(1-naphthoxy-methyl)-oxazolidine, a prodrug of propranolol, Kamal, A.; Rao, M.V.; Rao, A.B., Biochem. Pharmacol.1991, 41, 1393.
  • Enzymatic deprotection of methylthio-methyl esters: Synthesis of O-(carbomoyl) and O-(sulfamoyl)salicyclicacids, Kamal, A., Synth. Commun, 1991, 21, 1293.
  • Enantioselective hydrolysis of aryloxpropionic esters by bovine serum albumin: Enhancement in selectivity by beta-cyclodextrin, Kamal, A.; Ramalingam, T.; Venugopal, N., Tetrahedron Asymm. 1991, 2, 39.
  • Enzymatic approach to the synthesis of pyrrolo[1,4]benzodiazepine antibiotics, Kamal, A., J. Org. Chem. 1991, 56, 2237.
  • Metabolism of ethyl 2-carbamoyloxy-benzoate (4003/2), a prodrug of salicylic acid, carsalam and salicylamide, Kamal, A., Biochem. Pharmacol.1990, 40, 1669.
  • Recent advances in the synthetic uses of chlorocarbonyl isocyanate, Kamal, A., Heterocycles 1990, 31, 1337.
  • Enzymatic cyclizations mediated by ultrasonically stimulated Baker’s Yeast. Kamal, A.; Rao, M.V.; Rao, A.B., J. Chem. Soc.Perkin Trans.1990, 1, 2755.
  • Studies on the non-covalent interaction of pyrrolo[2,1-c][1,4]benzodiazepine-5,11-diones with DNA, Jones, G. B.; Davey, C. L.; Jenkins, T. C.; Kamal, A.; Kneale, G. G.; Neidle, S.; Thurston, D. E.; Webster, G. B., Anticancer Drug Design 1990, 5, 249.
  • Enzymatic cyclization involving intramolecular michaela by catalase: Formation of 2-methyl benzimidazoles, Kamal, A.; Hashim, R., Heterocycles 1990, 31, 969.
  • Enzymatic oxidative conversion of thio to oxo by Baker’s Yeast in thiocarbamates and thioureas, Kamal, A.; Rao, M.V.; Rao, A.B., Chemistry Lett. 1990, 655.
  • Efficient enzymatic cyclization of 2-(carbamoyloxy)- and 2-(sulfamoyloxy) benzonitriles by ultrasonically stimulated Baker’s Yeast, Kamal, A.; Rao, M.V.; Rao, A.B., Heterocycles 1990, 31, 577.
  • The synthesis of 1,2,4-triazolo[4,3-b] [1,2,4]benzodit-hiadiazine-5,5-dioxides: New class of angiotensin-converting enzyme inhibitors, Kamal, A.; Reddy, A.V.N.; Rao, A. B.; Sattur, P. B., J. Pharm. Pharmacol.(Suppl.) 1989, 41, 72.
  • Reaction of pyrrolo[2,1-c][1,4]benzodiazepine-2,5,11-triones with phosphorus oxychloride, Kamal, A.; Thurston, D. E., Tetrahedron Lett.1989, 30, 6221.
  • A novel enzymatic cyclization: Synthesis of imidazo-fused quinazoilinones by Baker’s Yeast, Kamal, A.; Sattur, P. B., J. Chem. Soc., Chem. Commun. 1989, 835.
  • Catalase-mediated cyclization: Synthesis of 3-Allyl-4-imino substituted 2(1H)-quinazolines and 1,3-benzoxazine-2(3H)-ones,                                                                         Kamal, A.; Sattur, P. B., Tetrahedron Lett. 1989, 30, 1133. 
  • Enzymatic cyclization of 2-(carbamoyl-oxy)/2-sulfomyloxy) benzoates/ 2-carbamoyloxybenzophenones with yeast and lipase, Kamal, A.; Rao, M. V.; Rao, A. B.; Sattur, P. B., Heterocycles 1989, 29, 1391.
  • Mass spectral studies of imidazo[1,2-b] [1,2,4]benzothiadiazine-5,5-dioxides, Vairamani,M.; Kamal, A.; Reddy, A.V.N.; Sattur, P. B., Org. Mass Spectrom. 1989, 24, 350.
  • Synthesis of 2-carbamoloxybenzoates as analgesic and antiflammatory agents, Kamal, A.; Rao, M.V.; Diwan, P. V.; Rao, A. B.; Sattur, P. B., Eur. J. Med. Chem.1988, 23, 487.
  • Cyclization of 2-(carbamoyloxy)- and 2-(sulfamoyloxy) benzoates mediated by liver microsomes, Kamal, A.; Rao, A. B.; Sattur, P.B., J. Org. Chem.1988, 53, 4112.
  • An efficient synthesis of 4-imino-2(1H)-quinazolinones, Reddy, A.V.N.; Kamal, A.; Sattur, P. B., Synth. Commun. 1988, 18, 525.
  • Chlorosulfonyl isocyanate: Anovel reagent for the synthesis of heterocycles, Kamal, A.; Sattur, P. B., Heterocycles 1987, 26, 1051.
  • Enzymatic cyclization of 2-carbamoyl-oxybenzoates: Formation of 2H-1,3-benzoxianine-2,4-(3H)-diones, Kamal, A.; Rao, A. B.; Sattur, P. B., Tetrahedron Lett. 1987, 28, 2425.
  • Synthesis of diazepino-fused heterocycles: Reactions with chlorobutyl isocyanate, Kamal, A.; Reddy, A.V.N.; Sattur, P. B., Heterocycles 1987, 26, 751. 
  • Synthesis and biological evaluation of 10-substitued imidazolo [4,5-b]-1,2,4-benzothiadiazine-5,5-dioxides and their 2,10-dihydro Analogues, Reddy, A.V.N.; Kamal, A.; Rao, A. B.; Sattur, P. B., Eur. J. Med. Chem. 1987, 22, 157.
  • Reactions with chlorosulfonyl/chlorocarbonyl isooctanes synthesis of pyrrolo[1,2,3,-de]-1,2,4-benzothiadiazine-3(2H)-one 1,1-dioxides and 1H-pyrrolo[3,2,1-ij]quinazoline-1,3[3H]-diones, Kamal, A.; Reddy, A.V.N.; Sattur, P. B., Heterocycles. 1986, 24, 3397.
  • Synthesis of 5H-dipyrido[1,2-a:3’2’-e]pyrimidin-5-one and 5H-pyrido[3’,2’:5,6]pyrimido[1,2-a]quinazoline-5-ones, Kamal, A.; Rao, M. V.; Sattur, P. B., Heterocycles.1986, 24, 3075.
  • A new facile synthesis of 3-amino-4-alkyl/arylsubstituted-2H-1,2,4-benzothiadiazine-1,1-dioxides, Reddy, A.V.N.; Kamal, A.; Sattur, P.B., Synthesis. 1986, 864.
  • Synthesis and biological evaluation of quinazolino[3,2-b]-1,2,4-benzothia-diazine-11,11-dioxides, Reddy, A.V.N.; Kamal, A.; Rao, A. B.; Sattur, P. B., Eur. J. Med. Chem.1986, 21, 177.
  • Synthesis and biological activity of 3-pyrazolyl-4-substituted-2H- 1,2,4-benzothiadianine 1,1-dioxides, Reddy, A.V.N.; Kamal, A.; Sattur, P. B., Ind. J. Chem.1985, 24B, 1295. 
  • A one pot synthesis of ring-fused 1,3,5-triazine2,4(3H)-diones: Reactions with chlorocarbonyl isocyanate, Kamal, A.; Sattur, P. B., Synthesis.1985, 892.
  • Synthesis and antiinflammatory activity of 4-aryl-2-1-(1-pyrazoyl) arylquinazolines, Kamal, A.; Sattur, P. B., Ind. J. Chem. 1985, 24B, 414.
  • Synthesis and biological activity of 1-subtituted 5-aryl-s-triazolo-[4,3-a]-quinazolines, Kamal, A.; Sattur, P. B., Ind. J. Chem. 1984, 23B, 1293.
  • Synthesi of 5-aryl-12H-quinazolino[3,2-a]quinazoline-12-ones as antiinflammatory agents, Kamal, A.; Sattur, P. B., Arch. Pharm. 1983, 316, 702.
  • Reactions with chlorosulfonyl isocyanate; formation of 2H-1,3-benzoxazine-2-ones, Kamal, A.; Sattur, P. B., Synth. Commun. 1982, 12(2), 157.
  • Mass spectral studies of 4-phenyl-2(1H)quinazolines, Kamal, A.; Sattur, P. B., Ind. J. Chem. 1981, B 20, 600. 
  • A facile synthesis of 1,2,3-benzoxathiazine 2,2-dioxides, Kamal, A.; Sattur, P. B., Synthesis 1981, 272.
  • A new route to 4-phenyl-2-(1H) quinazolines; reaction of 2-aminobenzophenones with chlorosulfonyl isocyanate, Kamal, A.; Rao, K. R.; Sattur, P. B., Synth. Commun. 1980, 10(10), 799.

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