| Visible light organophotoredox catalysis: a general approach to β-keto sulfoxidation of alkenes T Keshari, VK Yadav, VP Srivastava, LDS Yadav Green Chemistry 16 (8), 3986-3992, 2014 | 202 | 2014 |
| Biginelli reaction starting directly from alcohols VP Srivastava, LDS Yadav Tetrahedron Letters 51 (49), 6436-6438, 2010 | 87 | 2010 |
| Eosin Y catalyzed visible-light-driven aerobic oxidative cyclization of thioamides to 1, 2, 4-thiadiazoles VP Srivastava, AK Yadav, LDS Yadav Synlett 24 (04), 465-470, 2013 | 86 | 2013 |
| Garima and LDS Yadav VP Srivastava, R Patel Chem. Commun 46, 5808, 2010 | 72 | 2010 |
| An efficient conjugate hydrothiocyanation of chalcones with a task-specific ionic liquid LDS Yadav, R Patel, VK Rai, VP Srivastava Tetrahedron letters 48 (44), 7793-7795, 2007 | 69 | 2007 |
| Bromodimethylsulfonium bromide (BDMS): a useful reagent for conversion of aldoximes and primary amides to nitriles LDS Yadav, VP Srivastava, R Patel Tetrahedron Letters 50 (39), 5532-5535, 2009 | 55 | 2009 |
| Visible-light-mediated eosin Y catalyzed aerobic desulfurization of thioamides into amides AK Yadav, VP Srivastava, LDS Yadav New Journal of Chemistry 37 (12), 4119-4124, 2013 | 54 | 2013 |
| An easy access to functionalized allyl dithiocarbamates from Baylis–Hillman adducts in water LDS Yadav, R Patel, VP Srivastava Tetrahedron Letters 50 (12), 1335-1339, 2009 | 52 | 2009 |
| The first application of the Baylis–Hillman reaction in azetidine chemistry: a convenient synthesis of azetidine-3-carbonitriles/carboxylates LDS Yadav, VP Srivastava, R Patel Tetrahedron Letters 49 (39), 5652-5654, 2008 | 52 | 2008 |
| Visible-light-mediated efficient conversion of aldoximes and primary amides into nitriles AK Yadav, VP Srivastava, LDS Yadav RSC advances 4 (8), 4181-4186, 2014 | 50 | 2014 |
| Bromodimethylsulfonium bromide (BDMS)-catalyzed multicomponent synthesis of 3-aminoalkylated indoles DK Yadav, R Patel, VP Srivastava, G Watal, LDS Yadav Tetrahedron Letters 51 (43), 5701-5703, 2010 | 47 | 2010 |
| Bromodimethylsulfonium bromide (BDMS) in ionic liquid: a mild and efficient catalyst for Beckmann rearrangement LDS Yadav, VP Srivastava Tetrahedron Letters 51 (4), 739-743, 2010 | 44 | 2010 |
| An easy access to fluoroalkanes by deoxygenative hydrofluorination of carbonyl compounds via their tosylhydrazones AK Yadav, VP Srivastava, LDS Yadav Chemical Communications 49 (21), 2154-2156, 2013 | 43 | 2013 |
| The Beckmann rearrangement executed by visible-light-driven generation of Vilsmeier–Haack reagent VP Srivastava, AK Yadav, LDS Yadav Synlett 25 (05), 665-670, 2014 | 41 | 2014 |
| Bromodimethylsulfonium bromide (BDMS)-mediated Lossen rearrangement: synthesis of unsymmetrical ureas DK Yadav, AK Yadav, VP Srivastava, G Watal, LDS Yadav Tetrahedron Letters 53 (23), 2890-2893, 2012 | 39 | 2012 |
| An easy access to unsymmetrical ureas: a photocatalytic approach to the Lossen rearrangement AK Yadav, VP Srivastava, LDS Yadav RSC advances 4 (47), 24498-24503, 2014 | 36 | 2014 |
| Direct sulfonylation of Baylis-Hillman alcohols and diarylmethanols with TosMIC in ionic liquid-[Hmim] HSO4: an unexpected reaction VP Garima, LD Srivastava, S Yadav Tetrahedron Lett 51, 6436-6438, 2010 | 35 | 2010 |
| Iodide catalyzed synthesis of 2-aminobenzoxazoles via oxidative cyclodesulfurization of phenolic thioureas with hydrogen peroxide VK Yadav, VP Srivastava, LDS Yadav Tetrahedron Letters 59 (3), 252-255, 2018 | 34 | 2018 |
| The first example of ring expansion of N-tosylaziridines to 2-aroyl-N-tosylazetidines with nitrogen ylides in an aqueous medium VP Srivastava, LDS Yadav Green Chemistry 12 (8), 1460-1465, 2010 | 34 | 2010 |
| Ionic liquid [Hmim] HSO4-promoted one-pot oxidative conjugate addition of sulfur-centred nucleophiles to Baylis–Hillman adducts LDS Yadav, VP Srivastava, R Patel Tetrahedron Letters 49 (19), 3142-3146, 2008 | 33 | 2008 |
