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.

Reaction of lithioenamines with sulphinate esters. Stereospecific and stereoselective synthesis of beta-enamino and beta-imino sulphoxides / R. Annunziata, M. Cinquini, F. Cozzi, A. Restelli. - In: JOURNAL OF THE CHEMICAL SOCIETY. PERKIN TRANSACTIONS. I. - ISSN 0300-922X. - 1982(1982), pp. 1183-1186. [10.1039/P19820001183]

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

R. Annunziata;M. Cinquini;F. Cozzi;
1982

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.
Settore CHIM/06 - Chimica Organica
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/182400
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