Publication:
Concise syntheses of substituted indolizidine alkaloids via cyclization based on α-sulfinyl carbanions: preparation of (±)-indolizidines 167B and 209D, their epimers, and (±)-tashiromine

dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorSaisuree Prateeptongkumen_US
dc.contributor.authorSoontorn Chooprayoonen_US
dc.contributor.authorPatoomratana Tuchindaen_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-07-12T02:19:22Z
dc.date.available2018-07-12T02:19:22Z
dc.date.issued2008-03-03en_US
dc.description.abstract(±)-Indolizidines 167B and 209D, their epimers and (±)-tashiromine have been successfully synthesized, starting from simple γ- or α-lactams. The strategy involves the cyclization of α-sulfinyl carbanion onto the carbonyl group of the lactam ring as the key step, leading to the indolizidines containing the phenylsulfinyl group, which are used as precursors for the preparation of the title compounds. © 2008 Elsevier Ltd. All rights reserved.en_US
dc.identifier.citationTetrahedron. Vol.64, No.10 (2008), 2339-2347en_US
dc.identifier.doi10.1016/j.tet.2008.01.008en_US
dc.identifier.issn00404020en_US
dc.identifier.other2-s2.0-38649125571en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/18953
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=38649125571&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleConcise syntheses of substituted indolizidine alkaloids via cyclization based on α-sulfinyl carbanions: preparation of (±)-indolizidines 167B and 209D, their epimers, and (±)-tashiromineen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=38649125571&origin=inwarden_US

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