26065-78-1Relevant articles and documents
Manganese(iii)-promoted thiocarbonylation of alkylborates with disulfides: synthesis of aliphatic thioesters
Chen, Bo,Wu, Xiao-Feng
supporting information, p. 9654 - 9658 (2021/12/01)
A Mn(iii)-promoted thiocarbonylation procedure toward the synthesis of thioesters has been developed. By employing easily available disulfides and potassium alkyltrifluoroborates as the starting materials, and cheap and non-toxic Mn(OAc)3·2H2O as the promotor, a broad range of thioesters were synthesized in good to excellent yieldsviaradical intermediates.
A SIMPLE SYNTHESIS OF THIOL ESTERS FROM COPPER-I-MERCAPTIDES AND ACYL CHLORIDES
Reissig, Hans-Ulrich,Scherer, Bernadette
, p. 4259 - 4262 (2007/10/02)
Thiol esters are obtained from acyl chlorides and copper-I-mercaptides in excellent yields.