Issue 10, 1990

The synthesis of (±)-coronafacic acid by a tandem Wessely oxidation–Diels–Alder reaction sequence

Abstract

(±)-Coronafacic acid (9) has been synthesized from ethyl 5-(4-ethyl-2-hydroxyphenyl)pent-2-enoate (4)via a tandem Wessely oxidation–Diels–Alder reaction sequence.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 739-740

The synthesis of (±)-coronafacic acid by a tandem Wessely oxidation–Diels–Alder reaction sequence

N. K. Bhamare, T. Granger, T. S. Macas and P. Yates, J. Chem. Soc., Chem. Commun., 1990, 739 DOI: 10.1039/C39900000739

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