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Synthesis of naturally occurring anticancer agents by the Oxidative Spirocyclisation of Furans

Objetivo

The aim of this research is to apply organic synthetic methodology developed in the Robertson group to the synthesis of natural products and their analogues that are known to possess, or have the potential to possess, anticancer activity. The target compounds are all oxygen heterocycles that will be assembled by an oxidative spiro-cyclisation process from furan derivatives.

Ámbito científico (EuroSciVoc)

Tema(s)

Convocatoria de propuestas

FP6-2005-MOBILITY-5
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Régimen de financiación

EIF - Marie Curie actions-Intra-European Fellowships

Coordinador

THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Aportación de la UE
Sin datos
Coste total
Sin datos