Journal of the Chemical Society. Chemical communications p. 1628 - 1629 (1988)
Update date:2022-08-04
Topics:
Cotterill, Ian C.
Roberts, Stanley M.
Williams, Julian O.
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.
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