Publication:
Destannylative Pummerer-type rearrangement of 1-(tributylstannyl)-1-(phenylsulfinyl)- cyclopropane and -ethene.

Simple item page
dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorSrisamorn Sithikanchanakulen_US
dc.contributor.authorSujitra Khosavannaen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-08-10T08:54:13Z
dc.date.available2018-08-10T08:54:13Z
dc.date.issued1993-07-23en_US
dc.description.abstract1-(Tributylstannyl)-1-(phenylsulfinyl)-cyclopropane and -ethene were found to react with acyl chlorides to provide the corresponding 1-acyloxy-1-(phenylthio)-cyclopropanes and -ethenes. The reaction involves the Pummerer-type rearrangement with loss of the tributylstannyl group. © 1993.en_US
dc.identifier.citationTetrahedron. Vol.49, No.30 (1993), 6651-6660en_US
dc.identifier.doi10.1016/S0040-4020(01)81835-4en_US
dc.identifier.issn00404020en_US
dc.identifier.other2-s2.0-0027169362en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/22533
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0027169362&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-(tributylstannyl)-1-(phenylsulfinyl)- cyclopropane and -ethene.en_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0027169362&origin=inwarden_US

Files

Collections

Scopus 1991-2000