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.

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 (former - to 2024)
UEA Research Groups:	Faculty of Science > Research Groups > Synthetic Chemistry (former - to 2017) Faculty of Science > Research Groups > Chemistry of Materials and Catalysis
Depositing User:	Rachel Smith
Date Deposited:	20 Jun 2011 14:49
Last Modified:	24 Sep 2024 09:47
URI:	https://ueaeprints.uea.ac.uk/id/eprint/32876
DOI:	10.1055/s-2006-956461

Actions (login required)

View Item