An ytterbium-catalysed intramolecular aldehyde-ene reaction approach to the guaianolide and pseudoguaianolide diterpenoids: Synthesis of the guaiane skeleton

Bulman Page, Philip C., Gambera, Giovanni, Hayman, Colin M. and Edgar, Mark (2006) An ytterbium-catalysed intramolecular aldehyde-ene reaction approach to the guaianolide and pseudoguaianolide diterpenoids: Synthesis of the guaiane skeleton. Synlett (20). pp. 3411-3414. ISSN 0936-5214

Full text not available from this repository. (Request a copy)

Abstract

A convergent approach to a functionalised guaiane ring system, the core of the guaianolide and pseudoguaianolide diterpenes, is described. The synthesis utilises an intramolecular aldehydeene reaction as the key step.

Item Type: Article
Uncontrolled Keywords: sesquiterpene lactone,guaianolide,pseudoguaianolide,perhydroazulene,intramolecular ene reaction
Faculty \ School: Faculty of Science > School of Chemistry
Depositing User: Rachel Smith
Date Deposited: 20 Jun 2011 14:49
Last Modified: 21 Apr 2020 19:40
URI: https://ueaeprints.uea.ac.uk/id/eprint/32876
DOI: 10.1055/s-2006-956461

Actions (login required)

View Item View Item