Issue 24, 1979

Five-membered ring annelation via thermal rearrangement of β-cyclopropyl-αβ-unsaturated ketones: a new total synthesis of (±)-zizaene

Abstract

The bicyclic αβ-unsaturated ketone (2), conveniently prepared by thermal rearrangement of (1), is converted, via an 11-step sequence, into the tricyclic ketone (15), thus formally completing a new total synthesis of (±)-zizaene (3).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1979, 1138-1140

Five-membered ring annelation via thermal rearrangement of β-cyclopropyl-αβ-unsaturated ketones: a new total synthesis of (±)-zizaene

E. Piers and J. Banville, J. Chem. Soc., Chem. Commun., 1979, 1138 DOI: 10.1039/C39790001138

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements