Issue 58, 2016, Issue in Progress

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.

Graphical abstract: Silver-mediated oxidative trifluoromethylthiolation of cycloalkanols by C–C bond cleavage: a regioselective approach to distally trifluoromethylthiolated ketones

Supplementary files

Article information

Article type
Communication
Submitted
09 May 2016
Accepted
23 May 2016
First published
25 May 2016

RSC Adv., 2016,6, 52710-52714

Silver-mediated oxidative trifluoromethylthiolation of cycloalkanols by C–C bond cleavage: a regioselective approach to distally trifluoromethylthiolated ketones

F. Huang, Y. Wang, J. Sun, J. Xie, L. Qi and B. Zhang, RSC Adv., 2016, 6, 52710 DOI: 10.1039/C6RA11968A

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