Manat PohmakotrSrisamorn SithikanchanakulMahidol University2018-06-142018-06-141989-01-01Tetrahedron Letters. Vol.30, No.48 (1989), 6773-6776004040392-s2.0-0024849392https://repository.li.mahidol.ac.th/handle/20.500.14594/157181-(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.Mahidol UniversityBiochemistry, Genetics and Molecular BiologyChemistryPharmacology, Toxicology and PharmaceuticsDestannylative pummerer-type rearrangement of 1-(phenylsulfinyl)-1-(tributylstannyl)cyclopropaneArticleSCOPUS10.1016/S0040-4039(00)70673-3