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Destannylative pummerer-type rearrangement of 1-(phenylsulfinyl)-1-(tributylstannyl)cyclopropane

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dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorSrisamorn Sithikanchanakulen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-06-14T09:12:53Z
dc.date.available2018-06-14T09:12:53Z
dc.date.issued1989-01-01en_US
dc.description.abstract1-(Phenylsulfinyl)-1-(tributylstannyl)cyclopropane on treatment with acyl chlorides or alkyl chloroformate in refluxing dichloromethane afforded 1-acyloxy-1-phenylsulfenyl- and 1-alkoxycarbonyloxy-1-phenylsulfenylcyclopropanes, respectively. The reaction involves the Pummerer-type rearrangement with loss of tributylstannyl group. © 1989.en_US
dc.identifier.citationTetrahedron Letters. Vol.30, No.48 (1989), 6773-6776en_US
dc.identifier.doi10.1016/S0040-4039(00)70673-3en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-0024849392en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/15718
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0024849392&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleDestannylative pummerer-type rearrangement of 1-(phenylsulfinyl)-1-(tributylstannyl)cyclopropaneen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0024849392&origin=inwarden_US

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