Studies towards the total synthesis of lycoposerramine A. Synthesis of a model for the tetracyclic core

Elliott, Mark Christopher ORCID: https://orcid.org/0000-0003-0132-0818 and Paine, James S. 2009. Studies towards the total synthesis of lycoposerramine A. Synthesis of a model for the tetracyclic core. Organic & Biomolecular Chemistry 7 (17) , pp. 3455-3462. 10.1039/b909860g

Full text not available from this repository.

Abstract

Lycoposerramine A (1) is a pentacyclic alkaloid isolated in 2001 by Takayama and co-workers. A concise synthesis of a model compound 8 for the tetracyclic core of this natural product is described. Key steps include the desymmetrising free-radical cyclisation of compound 7 to give compound 18 and spirocyclisation of compound 26 to give compound 8. Earlier approaches using a novel high-yielding stereoselective anionic cyclisation of a cyclohexa-1,4-diene are also reported.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Chemistry
Publisher:	Royal Society of Chemistry
ISSN:	1477-0520
Last Modified:	17 Oct 2022 09:51
URI:	https://orca.cardiff.ac.uk/id/eprint/5932

Citation Data

Cited 16 times in Scopus. View in Scopus. Powered By Scopus® Data

Actions (repository staff only)

Edit Item