Title:
Total Syntheses of Kirkamide and N-acetyl ent-Conduramine B-1

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dc.contributor.authorChintam Narayana
dc.contributor.authorAshish Khanna
dc.contributor.authorPriti Kumari
dc.contributor.authorRam Sagar
dc.date.accessioned2026-02-07T10:42:45Z
dc.date.issued2021
dc.description.abstractThe second total synthesis of recently isolated new C7N aminocyclitol, kirkamide, has been developed. The enantiopure epoxide derived from N-acetylglucosamine in few steps was used as a synthon to accomplish the metal free synthesis of kirkamide and N-acetyl ent-conduramine B-1 in gram scale. The key synthetic steps involve stereoselective epoxidation, acid mediated regioselective epoxide ring opening followed by selective olefination. © 2020 Wiley-VCH GmbH
dc.identifier.doi10.1002/ajoc.202000608
dc.identifier.issn21935807
dc.identifier.urihttps://doi.org/10.1002/ajoc.202000608
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/38147
dc.publisherWiley-VCH Verlag
dc.subjectaminocyclitols
dc.subjectconduramine B-1
dc.subjectent-conduramine B-1
dc.subjectKirkamide
dc.subjectPeterson olefination
dc.subjectstereoselective epoxidation
dc.subjecttotal synthesis
dc.titleTotal Syntheses of Kirkamide and N-acetyl ent-Conduramine B-1
dc.typePublication
dspace.entity.typeArticle

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