Mukta Shaw - Publications

Affiliations: 
2015-2020 Indian Inst. of Technology - Patna 

7 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
2019 Kumar A, Shaw M. Additive Free Gold(III)-Catalyzed Stereoselective Synthesis of 2-Deoxyglycosides Using Phenylpropiolate Glycosides as Donors Mukta Shaw, and Amit Kumar. Chemistry, An Asian Journal. PMID 31381256 DOI: 10.1002/Asia.201900888  0.528
2019 Shaw M, Kumar A. Visible-Light-Mediated β-C(sp)-H Amination of Glycosylimidates: En Route to Oxazoline-Fused/Spiro Nonclassical Bicyclic Sugars. Organic Letters. PMID 30998381 DOI: 10.1021/Acs.Orglett.9B00763  0.449
2018 Shaw M, Thakur R, Kumar A. Gold(III)-Catalyzed Glycosylation using Phenylpropiolate Glycosides (PPGs): Phenylpropiolic Acid An Easily Separable and Reusable Leaving Group. The Journal of Organic Chemistry. PMID 30569713 DOI: 10.1021/Acs.Joc.8B02422  0.497
2017 Shaw M, Kumar Y, Thakur R, Kumar A. Electron-deficient pyridinium salts/thiourea cooperative catalyzed O-glycosylation via activation of O-glycosyl trichloroacetimidate donors. Beilstein Journal of Organic Chemistry. 13: 2385-2395. PMID 29181119 DOI: 10.3762/Bjoc.13.236  0.508
2017 Kumar Y, Jaiswal Y, Shaw M, Kumar A. Metal-Free Catalyst-Controlled Chemoselective Synthesis of Aryl α -Ketoesters and Primary α -Ketoamides from Aryl Acetimidates Chemistryselect. 2: 6143-6148. DOI: 10.1002/SLCT.201701322  0.505
2016 Kumar Y, Shaw M, Thakur R, Kumar A. Copper (II)-Mediated Aerobic Oxidation of Benzylimidates: Synthesis of Primary alpha-Ketoamides. The Journal of Organic Chemistry. PMID 27347744 DOI: 10.1021/Acs.Joc.6B01262  0.548
2016 Kumar Y, Shaw M, Thakur R, Kumar A. ChemInform Abstract: Copper(II)-Mediated Aerobic Oxidation of Benzylimidates: Synthesis of Primary α-Ketoamides. Cheminform. 47. DOI: 10.1002/CHIN.201651094  0.309
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