Synthesis of (-)-xialenon A by enantioselective alpha-deprotonation-rearrangement of a meso-epoxide

The first total synthesis of (-)-xialenon A was achieved via enantioselective transannular desymmetrisation of a substituted cycloctene oxide using an organolithium/(-)-α-isosparteine combination. Oxidation of the resulting bicyclo[3.3.0]octanol gave an enone which underwent stereoselective conjugat...

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Bibliografiska uppgifter
Huvudupphovsmän: Hodgson, D, Galano, J, Christlieb, M
Materialtyp: Journal article
Språk:English
Publicerad: 2003