Issue 23, 1985

A stereochemically controlled intramolecular Diels–Alder approach to the octahydronaphthalene fragment of dihydromevinolin

Abstract

An enantiospecific route to the octahydronaphthalene (22) from L-glutamic acid is described: the key step is the intramolecular Diels–Alder reaction (19) to (22).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 1662-1664

A stereochemically controlled intramolecular Diels–Alder approach to the octahydronaphthalene fragment of dihydromevinolin

A. H. Davidson, C. D. Floyd, A. J. Jones and P. L. Myers, J. Chem. Soc., Chem. Commun., 1985, 1662 DOI: 10.1039/C39850001662

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