Issue 19, 1976

New synthetic route to mono- and di-γδ-unsaturated NN-dialkylthionamides by the thio-Claisen rearrangement based on acyclic NN-dalkylthioamides

Abstract

Mono- and di-γδ-unsaturated NN-dialkylthiomides have been synthesized by a thio-Claisen rearrangement of α-amino-αβ-unsaturated sulphides derived from acyclic NN-dialkylthioamides.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1976, 776-777

New synthetic route to mono- and di-γδ-unsaturated NN-dialkylthionamides by the thio-Claisen rearrangement based on acyclic NN-dalkylthioamides

S. Takano, E. Yoshida, M. Hirama and K. Ogasawara, J. Chem. Soc., Chem. Commun., 1976, 776 DOI: 10.1039/C39760000776

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