Enantioselective total synthesis of (-)-xialenon A.
The first total synthesis of (-)-xialenon A (1) via conjugate allylation of a 1,5-cyclooctadiene-derived bicyclo[3.3.0]octenone 3 and an alpha'-hydroxylation on the more hinderd face of enone 9 using hypervalent iodine chemistry, is described.
Autores principales: | Hodgson, D, Galano, J, Christlieb, M |
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Formato: | Journal article |
Lenguaje: | English |
Publicado: |
2002
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