Silver-mediated oxidative trifluoromethylthiolation of cycloalkanols by C–C bond cleavage: a regioselective approach to distally trifluoromethylthiolated ketones†
Abstract
A novel method for the oxidative trifluoromethylthiolation of cycloalkanols by AgSCF3/K2S2O8 is described. The methodology provides an efficient and regioselective approach to distally trifluoromethylthiolated ketones in moderate to good yields. The reaction that is easily handled has a good functional-group tolerance and broad scope. Initial mechanistic studies indicate that the reaction may proceed via a radical pathway involving a tandem C(sp3)–C(sp3) bond cleavage and C(sp3)–SCF3 bond formation process.