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Intramolecular acylation of α-sulfinyl carbanion: a facile synthesis of (±)-pentenomycin I and (±)-epipentenomycin I.

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dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorSupatara Popuangen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-08-10T08:30:42Z
dc.date.available2018-08-10T08:30:42Z
dc.date.issued1991-01-07en_US
dc.description.abstract(±)-Pentenomycin I and (±)-epipentenomycin I were synthesized, starting from methyl 2,2-dimethyl-1,3-dioxolane-4-carboxylate. The key reaction involved the intramolecular acylation of α-sulfinyl carbanion and pyrolysis of the resulting product. © 1991.en_US
dc.identifier.citationTetrahedron Letters. Vol.32, No.2 (1991), 275-278en_US
dc.identifier.doi10.1016/0040-4039(91)80874-6en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-0026068713en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/21993
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0026068713&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleIntramolecular acylation of α-sulfinyl carbanion: a facile synthesis of (±)-pentenomycin I and (±)-epipentenomycin I.en_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0026068713&origin=inwarden_US

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