Manat PohmakotrSrisamorn SithikanchanakulSujitra KhosavannaMahidol University2018-08-102018-08-101993-07-23Tetrahedron. Vol.49, No.30 (1993), 6651-6660004040202-s2.0-0027169362https://repository.li.mahidol.ac.th/handle/20.500.14594/225331-(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.Mahidol UniversityBiochemistry, Genetics and Molecular BiologyChemistryPharmacology, Toxicology and PharmaceuticsDestannylative Pummerer-type rearrangement of 1-(tributylstannyl)-1-(phenylsulfinyl)- cyclopropane and -ethene.ArticleSCOPUS10.1016/S0040-4020(01)81835-4