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Synthetic studies on macrolactin A: construction of C4-C24 fragment
Marie Georgy1, Philippe Lesot, Jean-Marc Campagne
1ICSN-CNRS Avenue de la Terrasse, 91198 Gif-sur-Yvette, France.
The Journal of Organic Chemistry
|April 4, 2007
Abstract:
The preparation of the C4-C24 fragment of the macrolactin A is described. The adopted synthetic strategy involves two isomerizations to selectively construct the (8E,10Z) and (16E,18E) dienes, using a sequential Claisen rearrangement/allene isomerization and a Ph3P-catalyzed isomerization of an yne-one, respectively.
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