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Synthetic efforts toward the macrolactone core of Leucascandrolide A
Laurent Ferrié1, Lucie Boulard, Fabienne Pradaux
1Laboratoire de Chimie Organique, ESPCI, CNRS, 10 rue Vauquelin, 75231 Paris Cedex 05, France.
Abstract:
A chemoselective synthesis of 1, the macrocyclic core of leucascandrolide A, has been achieved by utilizing highly enantioselective allylmetalations, an enantioselective Noyori reduction of a propargylic ketone, and olefin metatheses as the key steps.
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