| 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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