Issue 19, 1985

A short, stereospecific synthesis of a morphine fragment via an intramolecular Diels–Alder reaction

Abstract

Intramolecular Diels–Alder reaction of trienes (8) gives the octahydroisoquinolones (10) which are readily converted into the biologically-active (12), a substructure of morphine.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 1362-1363

A short, stereospecific synthesis of a morphine fragment via an intramolecular Diels–Alder reaction

S. Handa, K. Jones, C. G. Newton and D. J. Williams, J. Chem. Soc., Chem. Commun., 1985, 1362 DOI: 10.1039/C39850001362

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