| A Versatile C–H Functionalization of Tetrahydroisoquinolines Catalyzed by Iodine at Aerobic Conditions† J Dhineshkumar, M Lamani, K Alagiri, KR Prabhu Organic letters 15 (5), 1092-1095, 2013 | 284 | 2013 |
| Regioselective synthesis of 4-substituted indoles via C–H activation: a ruthenium catalyzed novel directing group strategy V Lanke, K Ramaiah Prabhu Organic letters 15 (24), 6262-6265, 2013 | 185 | 2013 |
| CDC Reactions of N‐Aryl Tetrahydroisoquinolines Using Catalytic Amounts of DDQ: CH Activation under Aerobic Conditions K Alagiri, P Devadig, KR Prabhu Chemistry–A European Journal 17 (18), 5160-5164, 2012 | 168 | 2012 |
| Chemoselective Schmidt reaction mediated by triflic acid: selective synthesis of nitriles from aldehydes BV Rokade, KR Prabhu The Journal of organic chemistry 77 (12), 5364-5370, 2012 | 163 | 2012 |
| Recent advancements in dehydrogenative cross coupling reactions for CC bond formation BV Varun, J Dhineshkumar, KR Bettadapur, Y Siddaraju, K Alagiri, ... Tetrahedron Letters 58 (9), 803-824, 2017 | 158 | 2017 |
| Iodine-catalyzed amination of benzoxazoles: a metal-free route to 2-aminobenzoxazoles under mild conditions M Lamani, KR Prabhu The Journal of Organic Chemistry 76 (19), 7938-7944, 2011 | 158 | 2011 |
| NIS‐Catalyzed Reactions: Amidation of Acetophenones and Oxidative Amination of Propiophenones M Lamani, KR Prabhu Chemistry–A European Journal 18 (46), 14638-14642, 2012 | 156 | 2012 |
| Cross-hetero-dehydrogenative coupling reaction of phosphites: a catalytic metal-free phosphorylation of amines and alcohols J Dhineshkumar, KR Prabhu Organic letters 15 (23), 6062-6065, 2013 | 150 | 2013 |
| A Transition metal-free minisci reaction: Acylation of isoquinolines, quinolines, and quinoxaline Y Siddaraju, M Lamani, KR Prabhu The Journal of Organic Chemistry 79 (9), 3856-3865, 2014 | 147 | 2014 |
| Ru (II)-Catalyzed C–H Activation: Ketone-Directed Novel 1,4-Addition of Ortho C–H Bond to Maleimides KR Bettadapur, V Lanke, KR Prabhu Organic letters 17 (19), 4658-4661, 2015 | 145 | 2015 |
| Highly Regioselective C2-Alkenylation of Indoles Using the N-Benzoyl Directing Group: An Efficient Ru-Catalyzed Coupling Reaction V Lanke, KR Prabhu Organic letters 15 (11), 2818-2821, 2013 | 145 | 2013 |
| A concise synthesis of substituted thiourea derivatives in aqueous medium MR Maddani, KR Prabhu The Journal of organic chemistry 75 (7), 2327-2332, 2010 | 129 | 2010 |
| Electronic nature of ketone directing group as a key to control C-2 vs C-4 alkenylation of indoles V Lanke, KR Bettadapur, KR Prabhu Organic letters 18 (21), 5496-5499, 2016 | 125 | 2016 |
| C–H functionalization of tertiary amines by cross dehydrogenative coupling reactions: solvent-free synthesis of α-aminonitriles and β-nitroamines under aerobic condition K Alagiri, KR Prabhu Organic & Biomolecular Chemistry 10 (4), 835-842, 2012 | 121 | 2012 |
| Site-selective addition of maleimide to indole at the C-2 position: Ru (II)-catalyzed C–H activation V Lanke, KR Bettadapur, KR Prabhu Organic letters 17 (19), 4662-4665, 2015 | 115 | 2015 |
| Iodine-catalyzed cross dehydrogenative coupling reaction: a regioselective sulfenylation of imidazoheterocycles using dimethyl sulfoxide as an oxidant Y Siddaraju, KR Prabhu The Journal of Organic Chemistry 81 (17), 7838-7846, 2016 | 110 | 2016 |
| An efficient oxidation of primary azides catalyzed by copper iodide: a convenient method for the synthesis of nitriles M Lamani, KR Prabhu Angewandte Chemie International Edition 37 (49), 6622-6625, 2010 | 105 | 2010 |
| An oxidative cross-dehydrogenative-coupling reaction in water using molecular oxygen as the oxidant: vanadium catalyzed indolation of tetrahydroisoquinolines K Alagiri, GSR Kumara, KR Prabhu Chemical Communications 47 (42), 11787-11789, 2011 | 98 | 2011 |
| Rhodium (III)-catalyzed C–H activation at the C4-position of indole: switchable hydroarylation and oxidative Heck-type reactions of maleimides MS Sherikar, R Kapanaiah, V Lanke, KR Prabhu Chemical Communications 54 (79), 11200-11203, 2018 | 96 | 2018 |
| Pd-catalyzed hydroborylation of alkynes: a ligand controlled regioselectivity switch for the synthesis of α-or β-vinylboronates DP Ojha, KR Prabhu Organic Letters 18 (3), 432-435, 2016 | 93 | 2016 |
