Issue 6, 1974

Conformational preferences in some aryl substituted heterocyclic compounds exhibiting restricted internal rotation about C–N bonds

Abstract

X-Ray studies of the thermodynamically less stable (in solution) diastereoisomeric rotational isomer of 3-(2-bromophenyl)-5-methyl-2-thiohydantion (II) show that the bromine atom is transoid to the 5-methyl group.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 225-226

Conformational preferences in some aryl substituted heterocyclic compounds exhibiting restricted internal rotation about C–N bonds

P. H. Bird, L. D. Colebrook, A. R. Fraser and H. G. Giles, J. Chem. Soc., Chem. Commun., 1974, 225 DOI: 10.1039/C39740000225

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