Issue 30, 2005

2,2-Dimethyl cyclopentanones by acid catalyzed ring expansion of isopropenylcyclobutanols. A short synthesis of (±)-α-cuparenone and (±)-herbertene

Abstract

2,2-Dimethyl cyclopentanones are readily prepared by acid catalyzed ring expansion of isopropenylcyclobutanols; the method allows ready access to the family of sesquiterpenes cuparanes and herbertanes, as demonstrated by the synthesis of (±)-α-cuparenone and the direct precursor of (±)-herbertene.

Graphical abstract: 2,2-Dimethyl cyclopentanones by acid catalyzed ring expansion of isopropenylcyclobutanols. A short synthesis of (±)-α-cuparenone and (±)-herbertene

Supplementary files

Article information

Article type
Communication
Submitted
25 Apr 2005
Accepted
27 May 2005
First published
23 Jun 2005

Chem. Commun., 2005, 3853-3855

2,2-Dimethyl cyclopentanones by acid catalyzed ring expansion of isopropenylcyclobutanols. A short synthesis of (±)-α-cuparenone and (±)-herbertene

A. M. Bernard, A. Frongia, F. Secci and P. P. Piras, Chem. Commun., 2005, 3853 DOI: 10.1039/B505707H

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