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Conjugate addition to 5-phenylsulfinyl 2-substituted 2-cyclopentenones: A new route to 4,5-disubstituted 2-cyclopentenones

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dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorSupatara Popuangen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-06-14T09:06:27Z
dc.date.available2018-06-14T09:06:27Z
dc.date.issued1988-01-01en_US
dc.description.abstract4,5-Disubstituted 2-cyclopentenones have been prepared by conjugate addition of nitroalkanes and of organocopper reagents to 5-phenylsulfinyl 2-substituted 2-cyclopentenones, followed by pyrolysis. © 1988.en_US
dc.identifier.citationTetrahedron Letters. Vol.29, No.33 (1988), 4189-4192en_US
dc.identifier.doi10.1016/S0040-4039(00)80452-9en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-0142173083en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/15503
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0142173083&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleConjugate addition to 5-phenylsulfinyl 2-substituted 2-cyclopentenones: A new route to 4,5-disubstituted 2-cyclopentenonesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0142173083&origin=inwarden_US

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