Synthesis 2001(14): 2138-2142
DOI: 10.1055/s-2001-18063
PAPER
© Georg Thieme Verlag Stuttgart · New York

Total Synthesis of (±)-Kelsoene

Edward Piers*, Arturo Orellana
Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, British Columbia, V6T 1Z1Canada
Fax: +1(604)8222847; e-Mail: epier@interchange.ubc.ca;
Further Information

Publication History

Received 9 July 2001
Publication Date:
09 August 2004 (online)

Abstract

(±)-Kelsoene (1) has been synthesized in 15 steps from commercially available cyclopent-2-en-1-one. Key steps include (a) a methylenecyclopentane annulation of cyclopent-2-en-1-one using the bifunctional cuprate reagent lithium cyano(4-chlorobut-1-en-2-yl)cuprate and (b) a highly stereoselective [2+2]-photocycloaddition of ethylene to the bicyclic enone 10.

3

Previous literature reports have used different structural numbering systems for kelsoene. In this paper, we have chosen to number the kelsoene skeleton according to IUPAC protocol for tricyclic ring systems

28

This experiment was carried out using the CDCl3 solutions that had been employed to record the NMR spectra of compound 14