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Chandan Gharui - Publications

Affiliations: 
2015-2021 IIT Guwahati 
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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
2021 Gharui C, Parida C, Pan SC. Organocatalytic Asymmetric Addition of Aromatic α-Cyanoketones to -Quinone Methides: Synthesis of 3,4-Dihydrocoumarins and Tetrasubstituted Chromans. The Journal of Organic Chemistry. PMID 34464133 DOI: 10.1021/acs.joc.1c00435  0.525
2020 Gharui C, Prakash S, Chopra D, Pan SC. Organocatalytic asymmetric addition of thioglycolates to o-quinone methides: a route to 5-substituted-5H-benzoxathiepine-2(3H)-ones. Organic & Biomolecular Chemistry. PMID 32236238 DOI: 10.1039/D0Ob00568A  0.607
2019 Gharui C, Pan SC. Employment of α-nitroketones in organic synthesis. Organic & Biomolecular Chemistry. PMID 31070206 DOI: 10.1039/C9Ob00828D  0.703
2019 Mukhopadhyay S, Gharui C, Pan SC. Applications of Bifunctional Organocatalysts on ortho ‐Quinone Methides Asian Journal of Organic Chemistry. 8: 1970-1984. DOI: 10.1002/Ajoc.201900466  0.491
2018 Gharui C, Behera D, Pan SC. Organocatalytic Asymmetric Domino Michael/Acyl Transfer Reaction Between α -Nitroketones and in situ- Generated ortho -Quinone Methides: Route to 2-(1-Arylethyl)phenols Advanced Synthesis & Catalysis. 360: 4502-4508. DOI: 10.1002/Adsc.201801015  0.711
2017 Gharui C, Singh S, Pan SC. Chiral phosphoric acid catalyzed enantioselective annulation of acyclic enecarbamates to in situ-generated ortho-quinone methides. Organic & Biomolecular Chemistry. PMID 28858366 DOI: 10.1039/C7Ob01766A  0.691
2017 Maity R, Gharui C, Sil AK, Pan SC. Organocatalytic Asymmetric Michael/Hemiketalization/Retro-aldol Reaction of α-Nitroketones with Unsaturated Pyrazolones: Synthesis of 3-Acyloxy Pyrazoles. Organic Letters. PMID 28121452 DOI: 10.1021/Acs.Orglett.6B03823  0.696
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