Intramolecular Thia-anti-Michael Addition of a Sulfur Anion to Enones: A Regiospecific Approach to Multisubstituted Thiophene Derivatives

The intramolecular thia-anti-Michael addition starting from readily available α-alkenoyl-α‘-carbamoyl
ketene-(S,S)-acetals 1 containing a 1,3-dithiolane moiety was developed. In particular, in the presence of
aliphatic primary amines, a series of tetrasubstituted thiophene derivatives, 2-(alkylamino)-5-alkyl-4-hydroxythiophene-3-carboxamides 2, were synthesized via tandem fragmentation, substitution, and
intramolecular thia-anti-Michael addition reactions of 1, where amine played the dual roles of a base and
a nucleophile. The intramolecular thia-anti-Michael addition, as the key step, proceeded in a regiospecific
manner and showed a general scope to the β-substituents of enones 1. A possible mechanism for the
formation of the multisubstituted thiophenes was proposed. By this research, a new and efficient route
to various tetrasubstituted thiophene derivatives was created.