Issue 4, 1994

Diastereoselective anionic and radical conjugate addition on a chiral enone: a route to multichiral arrays

Abstract

1,4 Addition of several alkyl groups using cuprates and radicals on a conformationally biased chiral enone 3 derived from carbohydrate is described, showing essentially identical diastereoselection in anionic and radical processes and a dramatic influence of the alkyl group size on the sense of 1,2-asymmetric induction.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 399-401

Diastereoselective anionic and radical conjugate addition on a chiral enone: a route to multichiral arrays

P. Mayon, M. N. Euvrard, N. Moufid and Y. Chapleur, J. Chem. Soc., Chem. Commun., 1994, 399 DOI: 10.1039/C39940000399

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