Reaction of allenic, α-acetylenic, and propagylic sulphones with (–)-ephedrine affords enantiomerically pure 1,3-oxazolidine; the reaction proceeds via formation of the conjugated enamine and subsequent cyclization.

Stereospecific synthesis of 1,3-oxazolidine from allenic and acetylenic sulphones / M. Cinquini, F. Cozzi, M. Pelosi. - In: JOURNAL OF THE CHEMICAL SOCIETY. PERKIN TRANSACTIONS. I. - ISSN 0300-922X. - :0(1979), pp. 1430-1432.

Stereospecific synthesis of 1,3-oxazolidine from allenic and acetylenic sulphones

M. Cinquini;F. Cozzi;
1979

Abstract

Reaction of allenic, α-acetylenic, and propagylic sulphones with (–)-ephedrine affords enantiomerically pure 1,3-oxazolidine; the reaction proceeds via formation of the conjugated enamine and subsequent cyclization.
Settore CHIM/06 - Chimica Organica
JOURNAL OF THE CHEMICAL SOCIETY. PERKIN TRANSACTIONS. I
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/2434/182100
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