Issue 0, 1982

Reaction of lithioenamines with sulphinate esters. Stereospecific and stereoselective synthesis of β-enamino and β-imino sulphoxides

Abstract

Reaction of lithioenamines with (–)-menthyl (S)-toluene-p-sulphinate affords optically active β-enamino and/or β-imino sulphoxides, depending on the structure of the starting imine. The optical stability of both these classes of compounds is investigated.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1982, 1183-1186

Reaction of lithioenamines with sulphinate esters. Stereospecific and stereoselective synthesis of β-enamino and β-imino sulphoxides

R. Annunziata, M. Cinquini, A. Restelli and F. Cozzi, J. Chem. Soc., Perkin Trans. 1, 1982, 1183 DOI: 10.1039/P19820001183

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