Issue 19, 1989

Facial selectivity in the Diels–Alder reactions of cis-cyclohexa-3,5-diene-1,2-diol and derivatives with N-phenylmaleimide

Abstract

N-Phenylmaleimide adds to cis-cyclohexa-1,3-diene-1,2-diol and its derivatives preferentially to the face of the diene syn to the oxygen substituents; this effect is less pronounced in the more reactive, cyclic derivatives.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 1439-1440

Facial selectivity in the Diels–Alder reactions of cis-cyclohexa-3,5-diene-1,2-diol and derivatives with N-phenylmaleimide

J. R. Gillard and D. J. Burnell, J. Chem. Soc., Chem. Commun., 1989, 1439 DOI: 10.1039/C39890001439

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