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Meerwein-Ponndorf-Verley reaction of α-ketoepoxides. A stereocontrolled one-step synthesis of epoxy-1,3-diol monoesters

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dc.contributor.authorApiwat Barameeen_US
dc.contributor.authorNarongsak Chaichiten_US
dc.contributor.authorPoolsak Intaweeen_US
dc.contributor.authorChachanat Thebtaranonthen_US
dc.contributor.authorYodhathai Thebtaranonthen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherSilpakorn Universityen_US
dc.date.accessioned2018-08-10T08:30:39Z
dc.date.available2018-08-10T08:30:39Z
dc.date.issued1991-12-01en_US
dc.description.abstractLithium enolate 3, derived from ketoepoxide 1, adds to two molecules of an aldehyde with concomitant hydride transfer to produce 5 stereospecifically.en_US
dc.identifier.citationJournal of the Chemical Society, Chemical Communications. No.15 (1991), 1016-1017en_US
dc.identifier.doi10.1039/C39910001016en_US
dc.identifier.issn00224936en_US
dc.identifier.other2-s2.0-0025899334en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/21983
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0025899334&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleMeerwein-Ponndorf-Verley reaction of α-ketoepoxides. A stereocontrolled one-step synthesis of epoxy-1,3-diol monoestersen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0025899334&origin=inwarden_US

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