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Stereospecific triple Michael addition

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dc.contributor.authorChatchai Thanupranen_US
dc.contributor.authorChachanat Thebtaranonthen_US
dc.contributor.authorYodhathai Thebtaranonthen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-02-27T04:27:50Z
dc.date.available2018-02-27T04:27:50Z
dc.date.issued1986-01-01en_US
dc.description.abstractThe consecutive Michael addition of a nucleophile to an α -methylene cyclopentenone, thence to methyl acrylate, occurs readily and stereospecifically, yielding bicyclo-[2,2,1]-heptanone. The reaction represents the first example of a three-component triple conjugate addition process. © 1986.en_US
dc.identifier.citationTetrahedron Letters. Vol.27, No.20 (1986), 2295-2298en_US
dc.identifier.doi10.1016/S0040-4039(00)84512-8en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-0344389224en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/9674
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0344389224&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleStereospecific triple Michael additionen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0344389224&origin=inwarden_US

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