Additive-free synthesis of α-keton thiol esters via oxyacylthiolation of vinyl azides with thioacids and water
Abstract
An additive-free strategy has been developed for the synthesis of α-keton thiol esters through direct oxyacylthiolation of vinyl azides with thioacids and water. The C–S and C![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif) O bonds were formed in a one-pot operation via a radical reaction pathway. A number of α-keton thiol esters could be efficiently obtained in good yields with broad substrate scope and good functional group tolerance.
O bonds were formed in a one-pot operation via a radical reaction pathway. A number of α-keton thiol esters could be efficiently obtained in good yields with broad substrate scope and good functional group tolerance.
 
                




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