Issue 22, 1996

Asymmetric cyclization of unsaturated alcohols and carboxylic acids with camphor-based selenium electrophiles

Abstract

The diastereoselective cyclization of a series of unsaturated alcohols and carboxylic acids was achieved with chiral camphor-based selenenyl chlorides, of which the spiro-oxazolidinone 3c proved the most effective.

Article information

Article type
Paper

Chem. Commun., 1996, 2567-2568

Asymmetric cyclization of unsaturated alcohols and carboxylic acids with camphor-based selenium electrophiles

T. G. Back and B. P. Dyck, Chem. Commun., 1996, 2567 DOI: 10.1039/CC9960002567

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