Issue 1, 1991

Reaction of cyclopent-2-en-1-one ethylene acetal with dienophiles via its ring-opened enol ether form. Single step synthesis of norbornan-2-one ethylene acetals

Abstract

Cyclopent-2-en-1-one ethylene acetal undergoes Diels–Alder reaction with a variety of dienophiles via its ring-opened enol ether, 2-(2-hydroxyethoxy)cyclopenta-1,3-diene, under neutral conditions to give norbornan-2-one ethylene acetals.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1991, 37-38

Reaction of cyclopent-2-en-1-one ethylene acetal with dienophiles via its ring-opened enol ether form. Single step synthesis of norbornan-2-one ethylene acetals

M. Ohkita, T. Tsuji and S. Nishida, J. Chem. Soc., Chem. Commun., 1991, 37 DOI: 10.1039/C39910000037

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