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Destannylative acylation of 1-(tributylstannyl)-1-(phenylsulfonyl)-cyclopropane and -ethene.

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dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorSujitra Khosavannaen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-08-10T08:54:16Z
dc.date.available2018-08-10T08:54:16Z
dc.date.issued1993-01-01en_US
dc.description.abstractThe reaction of α-stannyl sulfones 1 and 2 with acyl chlorides in refluxing toluene, leading to 1-acyl-1-(phenylsulfonyl)cyclopropanes 3 and the labile 1-acyl-1-(phenylsulfonyl)ethenes 4, is described. © 1993.en_US
dc.identifier.citationTetrahedron. Vol.49, No.29 (1993), 6483-6488en_US
dc.identifier.doi10.1016/S0040-4020(01)80162-9en_US
dc.identifier.issn00404020en_US
dc.identifier.other2-s2.0-0027205528en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/22544
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0027205528&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleDestannylative acylation of 1-(tributylstannyl)-1-(phenylsulfonyl)-cyclopropane and -ethene.en_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0027205528&origin=inwarden_US

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