Issue 8, 1985

A novel synthesis of nezukone via the rearrangement of a bicyclic isomer: evidence for the intermediacy of heptafulvenes

Abstract

The bicyclic methylenecyclopropane (2) is converted into nezukone (1) in 61% yield; evidence is presented which suggested heptafulvenes are involved in this conversion.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 514-515

A novel synthesis of nezukone via the rearrangement of a bicyclic isomer: evidence for the intermediacy of heptafulvenes

M. G. Banwell, G. L. Gravatt and C. E. F. Rickard, J. Chem. Soc., Chem. Commun., 1985, 514 DOI: 10.1039/C39850000514

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