Issue 24, 1988

Diels–Alder reactions involving cis-1,2-isopropylidenedioxycyclohexa-3,5-diene and enzymatic resolution of one of the adducts

Abstract

cis-1,2-Isopropylidenedioxycyclohexa-3,5-diene undergoes Diels–Alder [4 + 2] cycloaddition reactions with a variety of dienophiles including dimethyl acetylenedicarboxylate; the adduct formed with the latter dienophile was hydrolysed stereoselectively by pig liver esterase.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 1628-1629

Diels–Alder reactions involving cis-1,2-isopropylidenedioxycyclohexa-3,5-diene and enzymatic resolution of one of the adducts

I. C. Cotterill, S. M. Roberts and J. O. Williams, J. Chem. Soc., Chem. Commun., 1988, 1628 DOI: 10.1039/C39880001628

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