| Spiro [pyrrolidine-3, 3-oxindole] as potent anti-breast cancer compounds: Their design, synthesis, biological evaluation and cellular target identification S Hati, S Tripathy, PK Dutta, R Agarwal, R Srinivasan, A Singh, S Singh, ... Scientific Reports 6 (1), 32213, 2016 | 84 | 2016 |
| Design, synthesis and evaluation of thiohydantoin derivatives as potent topoisomerase I (Top1) inhibitors with anticancer activity P Majumdar, C Bathula, SM Basu, SK Das, R Agarwal, S Hati, A Singh, ... European journal of medicinal chemistry 102, 540-551, 2015 | 79 | 2015 |
| Bicyclic and bridged nitrogen heterocycles W Chen, P Zhang, JB Aggen, DJ Dairaghi, AMK Pennell, S Sen, ... US Patent 7,435,831, 2008 | 58 | 2008 |
| Accessing benzimidazoles via a ring distortion strategy: an oxone mediated tandem reaction of 2-Aminobenzylamines S Hati, P Kumar Dutta, S Dutta, P Munshi, S Sen Organic letters 18 (13), 3090-3093, 2016 | 49 | 2016 |
| Substituted piperazines AMK Pennell, JB Aggen, JJK Wright, S Sen, BE Mcmaster, DJ Dairaghi, ... US Patent 7,842,693, 2010 | 45 | 2010 |
| Oxidative dehydrogenation of C–C and C–N bonds: A convenient approach to access diverse (dihydro) heteroaromatic compounds S Hati, U Holzgrabe, S Sen Beilstein Journal of Organic Chemistry 13 (1), 1670-1692, 2017 | 43 | 2017 |
| Directing-group-assisted manganese-catalyzed cyclopropanation of indoles PK Dutta, J Chauhan, MK Ravva, S Sen Organic letters 21 (7), 2025-2028, 2019 | 40 | 2019 |
| Synthesis of quinazolines and dihydroquinazolines: o-iodoxybenzoic acid mediated tandem reaction of o-aminobenzylamine with aldehydes S Hati, S Sen Synthesis 48 (09), 1389-1398, 2016 | 38 | 2016 |
| Indole based antimalarial compounds targeting the melatonin pathway: their design, synthesis and biological evaluation T Luthra, AK Nayak, S Bose, S Chakrabarti, A Gupta, S Sen European journal of medicinal chemistry 168, 11-27, 2019 | 36 | 2019 |
| Cobalt-Catalyzed, Hydroxyl-Assisted C–H Bond Functionalization: Access to Diversely Substituted Polycyclic Pyrans PK Dutta, MK Ravva, S Sen The Journal of Organic Chemistry 84 (3), 1176-1184, 2019 | 35 | 2019 |
| Design, synthesis and biological evaluation of small molecules as potent glucosidase inhibitors S Hati, SM Madurkar, C Bathula, C Thulluri, R Agarwal, FA Siddiqui, ... European Journal of Medicinal Chemistry 100, 188-196, 2015 | 34 | 2015 |
| Blue LED mediated intramolecular C–H functionalization and cyclopropanation of tryptamines: synthesis of azepino [4, 5-b] indoles and natural product inspired polycyclic indoles J Chauhan, MK Ravva, L Gremaud, S Sen Organic letters 22 (11), 4537-4541, 2020 | 32 | 2020 |
| N-Bromo-succinimide promoted synthesis of β-carbolines and 3, 4-dihydro-β-carbolines from tetrahydro-β-carbolines S Hati, S Sen Tetrahedron Letters 57 (9), 1040-1043, 2016 | 32 | 2016 |
| Substituted piperazines A Pennell, J Aggen, JJ Wright, S Sen, B McMaster, D Dairaghi, W Chen, ... US Patent App. 10/979,882, 2005 | 32 | 2005 |
| Harnessing Autoxidation of Aldehydes: In Situ Iodoarene Catalyzed Synthesis of Substituted 1,3,4-Oxadiazole, in the Presence of Molecular Oxygen J Chauhan, MK Ravva, S Sen Organic letters 21 (16), 6562-6565, 2019 | 31 | 2019 |
| Enantioselective synthesis of spirooxoindoles via chiral auxiliary (bicyclic lactam) controlled SN Ar reactions S Sen, VR Potti, R Surakanti, YLN Murthy, R Pallepogu Organic & Biomolecular Chemistry 9 (2), 358-360, 2011 | 30 | 2011 |
| Diaryl ethers using fischer chromium carbene mediated benzannulation SR Pulley, S Sen, A Vorogushin, E Swanson Organic Letters 1 (11), 1721-1723, 1999 | 30 | 1999 |
| Blue LED-mediated N–H insertion of indoles into aryldiazoesters at room temperature in batch and flow: reaction kinetics, density functional theory, and mechanistic study D Maiti, R Das, S Sen The Journal of Organic Chemistry 86 (3), 2522-2533, 2021 | 29 | 2021 |
| A novel library of -arylketones as potential inhibitors of α-glucosidase: Their design, synthesis, in vitro and in vivo studies T Luthra, R Agarwal, M Estari, U Adepally, S Sen Scientific reports 7 (1), 13246, 2017 | 29 | 2017 |
| A diversity oriented synthesis of natural product inspired molecular libraries J Chauhan, T Luthra, R Gundla, A Ferraro, U Holzgrabe, S Sen Organic & Biomolecular Chemistry 15 (43), 9108-9120, 2017 | 29 | 2017 |
