Issue 14, 1979

Regio- and stereo-controlled total synthesis of the stemodane nucleus; an unusual diterpene skeleton

Abstract

Photocatalysed intramolecular oxidative phenol coupling and subsequent regiospecific intramolecular C–H insertion have been utilized as the key steps for a totally synthetic route to the unusual tetracyclic diterpene, deoxystemodin (1).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1979, 622-623

Regio- and stereo-controlled total synthesis of the stemodane nucleus; an unusual diterpene skeleton

S. Chatterjee, J. Chem. Soc., Chem. Commun., 1979, 622 DOI: 10.1039/C39790000622

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