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J Org Chem ; 84(19): 12542-12552, 2019 10 04.
Article in English | MEDLINE | ID: mdl-31462047

ABSTRACT

Enol ethers are formed by radical decarboxylation of α-alkoxy ß-phenylthio acids via the corresponding Barton esters. The phenylthio acids were usually made by the known regioselective reaction of α,ß-epoxy acids with PhSH in the presence of InCl3, followed by O-alkylation of the resulting alcohol. In one case, thiol addition to an α,ß-unsaturated ethoxymethyl ester was used.

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