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Diastereoselectivity in Michael additions to a pyrrolidinyl enone

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dc.contributor.authorRoderick W. Batesen_US
dc.contributor.authorPalangpon Kongsaereeen_US
dc.contributor.otherChulalongkorn Universityen_US
dc.contributor.otherChulabhorn Research Instituteen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-09-07T08:49:47Z
dc.date.available2018-09-07T08:49:47Z
dc.date.issued1999-01-01en_US
dc.description.abstractMichael additions of stabilized carabanions to an α-pyrrolidinylenone are highly diastereoselective. Epoxidation is similarly selective.en_US
dc.identifier.citationSynlett. No.8 (1999), 1307-1309en_US
dc.identifier.doi10.1055/s-1999-2825en_US
dc.identifier.issn09365214en_US
dc.identifier.other2-s2.0-0032806759en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/25387
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0032806759&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleDiastereoselectivity in Michael additions to a pyrrolidinyl enoneen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0032806759&origin=inwarden_US

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