Chlorolysis of beta-functionalized alkyl polyfluoroalkenyl sulfides giving rise to beta-functionalized polyfluoroalkenesulfenyl chlorides was examined. beta-Cyano-containing sulfenyl chlorides underwent intramolecular cyclization at the nitrile group to form substituted isothiazoles.
Chlorolysis of beta-functionalized alkyl polyfluoroalkenyl sulfides giving rise to beta-functionalized polyfluoroalkenesulfenyl chlorides was examined. beta-Cyano-containing sulfenyl chlorides underwent intramolecular cyclization at the nitrile group to form substituted isothiazoles.
Chlorolysis of beta-functionalized alkyl polyfluoroalkenyl sulfides giving rise to beta-functionalized polyfluoroalkenesulfenyl chlorides was examined. beta-Cyano-containing sulfenyl chlorides underwent intramolecular cyclization at the nitrile group to form substituted isothiazoles.