Issue 16, 1996

Asymmetry in the boronic acid Mannich reaction: diastereocontrolled addition to chiral iminium species derived from aldehydes and (S)-5-phenylmorpholin-2-one

Abstract

(S)-5-Phenylmorpholin-2-one† and a range of aliphatic aldehydes form chiral iminium intermediates which undergo diastereoselective Mannich reactions with 2-furylboronic acid. Single crystal X-ray analysis of methylated derivative 4 derived from major adduct 2g confirms the stereochemical course of the reaction.

Article information

Article type
Paper

Chem. Commun., 1996, 1953-1954

Asymmetry in the boronic acid Mannich reaction: diastereocontrolled addition to chiral iminium species derived from aldehydes and (S)-5-phenylmorpholin-2-one

L. M. Harwood, G. S. Currie, M. G. B. Drew and R. W. A. Luke, Chem. Commun., 1996, 1953 DOI: 10.1039/CC9960001953

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