Abstract
Abstract Sulfenylation of enaminone anions on Cα, with alkyl and aryl sulfenyl chlorides or disulfides gave 1-alkyl (aryl) thioacetyl-2-styrylamines. The starting enaminones for the sequence may conveniently be prepared in one step from a substituted phenylacetone and N. N-dimethylformamide dimethyl acetal.
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