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Intramolecular acylation of α-sulfinyl carbanion: A new general route to 5-substituted Δ<sup>2</sup>cyclopentenones

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dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorPranee Phinyocheepen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-10-12T07:40:16Z
dc.date.available2018-10-12T07:40:16Z
dc.date.issued1984-01-01en_US
dc.description.abstractA general method for the preparation of 5-substituted Δ2-cyclopentenones via the intramolecular acylation of αot-sulfinyl carbanions has been demonstrated. © 1984.en_US
dc.identifier.citationTetrahedron Letters. Vol.25, No.21 (1984), 2249-2252en_US
dc.identifier.doi10.1016/S0040-4039(01)80224-0en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-0343046278en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/30579
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0343046278&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 new general route to 5-substituted Δ<sup>2</sup>cyclopentenonesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0343046278&origin=inwarden_US

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