19 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Gond KK, Maddani MR. Addition of sulfonylphthalides to -quinone methides: Selective 1,6-additions and oxidative annulations. Organic & Biomolecular Chemistry. 21: 2504-2508. PMID 36897072 DOI: 10.1039/d2ob02134j  0.568
2021 Rai V, P K, Harmalkar SS, Dhuri SN, Maddani MR. 1,6-Addition of 1,2,3-NH triazoles to -quinone methides: Facile access to highly selective N and N substituted triazoles. Organic & Biomolecular Chemistry. PMID 34908078 DOI: 10.1039/d1ob01717a  0.475
2020 Sorabad GS, Maddani MR. Facile, regioselective oxidative selenocyanation of N-aryl enaminones under transition-metal-free conditions New Journal of Chemistry. 44: 2222-2227. DOI: 10.1039/C9Nj05845A  0.804
2020 Rai V, Sorabad GS, Maddani MR. CuX 2 Mediated Facile Halocyclization of N ‐Allyl Thioureas Chemistryselect. 5: 6565-6569. DOI: 10.1002/slct.202000593  0.268
2019 Sorabad GS, Maddani MR. Metal free, facile sulfenylation of ketene dithioacetals catalyzed by an HBr–DMSO system New Journal of Chemistry. 43: 5996-6000. DOI: 10.1039/C9Nj00925F  0.787
2019 Sorabad GS, Maddani MR. Metal-free, green and efficient oxidative α halogenation of enaminones by halo acid and DMSO New Journal of Chemistry. 43: 6563-6568. DOI: 10.1039/C8Nj06412A  0.806
2019 Sorabad GS, Maddani MR. Metal‐Free, Facile Synthesis of Sulfenylated Chromones and Indoles Promoted by an Aqueous HBr−DMSO System Asian Journal of Organic Chemistry. 8: 1336-1343. DOI: 10.1002/Ajoc.201900402  0.769
2014 Maddani MR, Fiaud JC, Kagan HB. Stoichiometric Kinetic Resolution Reactions Separation of Enantiomers: Synthetic Methods. 13-74. DOI: 10.1002/9783527650880.ch2  0.602
2011 Prabhu K, Maddani M. Metal-Free Deprotection of Terminal Acetonides by Using tert-Butyl Hydroperoxide in Aqueous Medium Synlett. 2011: 821-825. DOI: 10.1055/S-0030-1259917  0.789
2011 Maddani MR, Prabhu KR. ChemInform Abstract: Metal-Free Deprotection of Terminal Acetonides by Using tert-Butyl Hydroperoxide in Aqueous Medium. Cheminform. 42: no-no. DOI: 10.1002/chin.201130206  0.716
2011 Maddani MR, Prabhu KR. ChemInform Abstract: Dioxomolybdenum Reagents in Organic Synthesis: Utility of Redox Capability to Design Reduction and Oxidation Cheminform. 42: no-no. DOI: 10.1002/chin.201129215  0.752
2010 Maddani MR, Prabhu KR. A concise synthesis of substituted thiourea derivatives in aqueous medium. The Journal of Organic Chemistry. 75: 2327-32. PMID 20201494 DOI: 10.1021/Jo1001593  0.766
2010 Maddani MR, Moorthy SK, Prabhu KR. Chemoselective reduction of azides catalyzed by molybdenum xanthate by using phenylsilane as the hydride source Tetrahedron. 66: 329-333. DOI: 10.1016/J.Tet.2009.10.093  0.747
2010 Maddani MR, Moorthy SK, Prabhu KR. ChemInform Abstract: Chemoselective Reduction of Azides Catalyzed by Molybdenum Xanthate by Using Phenylsilane as the Hydride Source. Cheminform. 41. DOI: 10.1002/CHIN.201018066  0.716
2008 Maddani M, Prabhu KR. Corrigendum to “A chemoselective aerobic oxidation of benzylic azides catalyzed by molybdenum xanthate in an aqueous medium” [Tetrahedron Lett. 49 (2008) 4526] Tetrahedron Letters. 49: 5436. DOI: 10.1016/J.Tetlet.2008.07.001  0.786
2008 Maddani M, Prabhu KR. A chemoselective aerobic oxidation of benzylic azides catalyzed by molybdenum xanthate in an aqueous medium Tetrahedron Letters. 49: 4526-4530. DOI: 10.1016/J.Tetlet.2008.05.047  0.791
2008 Maddani M, Prabhu KR. ChemInform Abstract: A Chemoselective Aerobic Oxidation of Benzylic Azides Catalyzed by Molybdenum Xanthate in an Aqueous Medium. Cheminform. 39. DOI: 10.1002/CHIN.200842063  0.781
2008 Maddani M, Prabhu KR. ChemInform Abstract: A Convenient Method for the Synthesis of Substituted Thioureas. Cheminform. 39. DOI: 10.1002/CHIN.200801054  0.738
2007 Maddani M, Prabhu KR. A convenient method for the synthesis of substituted thioureas Tetrahedron Letters. 48: 7151-7154. DOI: 10.1016/J.Tetlet.2007.07.212  0.799
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