Issue 11, 1980

Stereoselectivity of ring closure of substituted hex-5-enyl radicals

Abstract

1,5-Ring closure of 1- or 3-substituted hex-5-enyl radicals affords mainly cis-disubstituted cyclic products, whereas 2- or 4-substituted species give mainly trans-products; the significance of this stereoselectivity is demonstrated in the formation of the norbornane system from acyclic precursors.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1980, 484-485

Stereoselectivity of ring closure of substituted hex-5-enyl radicals

A. L. J. Beckwith, T. Lawrence and A. K. Serelis, J. Chem. Soc., Chem. Commun., 1980, 484 DOI: 10.1039/C39800000484

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