| An efficient method for cleavage of epoxides with aromatic amines G Sekar, VK Singh The Journal of organic chemistry 64 (1), 287-289, 1999 | 202 | 1999 |
| Cu-catalyzed one-pot synthesis of unsymmetrical diaryl thioethers by coupling of aryl halides using a thiol precursor DJC Prasad, G Sekar organic letters 13 (5), 1008-1011, 2011 | 187 | 2011 |
| Aerobic, Chemoselective Oxidation of Alcohols to Carbonyl Compounds Catalyzed by a DABCO‐Copper Complex under Mild Conditions S Mannam, SK Alamsetti, G Sekar Advanced Synthesis & Catalysis 349 (14‐15), 2253-2258, 2007 | 183 | 2007 |
| Asymmetric Kharasch Reaction: Catalytic Enantioselective Allylic Oxidation of Olefins Using Chiral Pyridine Bis(diphenyloxazoline)−Copper Complexes and tert-Butyl … G Sekar, A DattaGupta, VK Singh The Journal of Organic Chemistry 63 (9), 2961-2967, 1998 | 151 | 1998 |
| General, mild, and intermolecular Ullmann-type synthesis of diaryl and alkyl aryl ethers catalyzed by diol− copper (I) complex AB Naidu, EA Jaseer, G Sekar The Journal of Organic Chemistry 74 (10), 3675-3679, 2009 | 143 | 2009 |
| Catalytic enantioselective cyclopropanation of olefins using carbenoid chemistry VK Singh, A DattaGupta, G Sekar Synthesis 1997 (02), 137-149, 1997 | 135 | 1997 |
| Straightforward strategies for the preparation of NH-sulfoximines: a serendipitous story JA Bull, L Degennaro, R Luisi Synlett 28 (19), 2525-2538, 2017 | 126 | 2017 |
| Recent applications of α-carbonyl sulfoxonium ylides in rhodium-and iridium-catalyzed C–H functionalizations X Wu, S Sun, JT Yu, J Cheng Synlett 30 (01), 21-29, 2019 | 105 | 2019 |
| D-Glucose as green ligand for selective copper-catalyzed phenol synthesis from aryl halides with an easy catalyst removal KG Thakur, G Sekar Chemical communications 47 (23), 6692-6694, 2011 | 103 | 2011 |
| An efficient intermolecular C (aryl)–S bond forming reaction catalyzed by BINAM–copper (II) complex DJC Prasad, AB Naidu, G Sekar Tetrahedron letters 50 (13), 1411-1415, 2009 | 98 | 2009 |
| An efficient copper (II)-catalyzed synthesis of benzothiazoles through intramolecular coupling-cyclization of N-(2-chlorophenyl) benzothioamides EA Jaseer, DJC Prasad, A Dandapat, G Sekar Tetrahedron Letters 51 (38), 5009-5012, 2010 | 97 | 2010 |
| Highly Efficient Copper-Catalyzed Domino Ring Opening and Goldberg Coupling Cyclization for the Synthesis of 3,4-Dihydro-2H-1,4-benzoxazines RK Rao, AB Naidu, G Sekar Organic Letters 11 (9), 1923-1926, 2009 | 93 | 2009 |
| Efficient method for cleavage of aziridines with aromatic amines G Sekar, VK Singh The Journal of Organic Chemistry 64 (7), 2537-2539, 1999 | 92 | 1999 |
| CuCl catalyzed oxidation of aldehydes to carboxylic acids with aqueous tert-butyl hydroperoxide under mild conditions S Mannam, G Sekar Tetrahedron Letters 49 (6), 1083-1086, 2008 | 89 | 2008 |
| Metal-catalyzed C–S bond formation using sulfur surrogates N Sundaravelu, S Sangeetha, G Sekar Organic & Biomolecular Chemistry 19 (7), 1459-1482, 2021 | 87 | 2021 |
| A Versatile and One-Pot Strategy to Synthesize α-Amino Ketones from Benzylic Secondary Alcohols Using N-Bromosuccinimide S Guha, V Rajeshkumar, SS Kotha, G Sekar Organic letters 17 (3), 406-409, 2015 | 87 | 2015 |
| An efficient copper (I) complex catalyzed Sonogashira type cross-coupling of aryl halides with terminal alkynes KG Thakur, EA Jaseer, AB Naidu, G Sekar Tetrahedron Letters 50 (24), 2865-2869, 2009 | 84 | 2009 |
| CBr4 as a Halogen Bond Donor Catalyst for the Selective Activation of Benzaldehydes to Synthesize α,β-Unsaturated Ketones I Kazi, S Guha, G Sekar Organic letters 19 (5), 1244-1247, 2017 | 81 | 2017 |
| Copper-Catalyzed Domino Synthesis of 2-Arylthiochromanones through Concomitant C–S Bond Formations Using Xanthate as Sulfur Source S Sangeetha, P Muthupandi, G Sekar Organic letters 17 (24), 6006-6009, 2015 | 77 | 2015 |
| D-Glucosamine as a green ligand for copper catalyzed synthesis of primary aryl amines from aryl halides and ammonia KG Thakur, D Ganapathy, G Sekar Chemical Communications 47 (17), 5076-5078, 2011 | 77 | 2011 |
Vinod K SinghProfessor of Chemistry, IIT Kanpur在 iitk.ac.in 的电子邮件经过验证
