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Intramolecular acylation of α-sulfinyl carbanion a new general route to 5-methylene-2-cyclopentenones

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dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorSirirat Chancharuneeen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-10-12T07:40:23Z
dc.date.available2018-10-12T07:40:23Z
dc.date.issued1984-01-01en_US
dc.description.abstractA convenient synthesis of 5-methylene-2-cyclopentenones including Methylenomycin B involving the intramolecular acylation of α-sulfinyl carbanion followed by methylation and pyrolysis is described. © 1984.en_US
dc.identifier.citationTetrahedron Letters. Vol.25, No.37 (1984), 4141-4144en_US
dc.identifier.doi10.1016/S0040-4039(01)90204-7en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-0142173082en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/30584
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0142173082&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-methylene-2-cyclopentenonesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0142173082&origin=inwarden_US

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