| Literature DB >> 18229938 |
Laurent Ferrié1, Lucie Boulard, Fabienne Pradaux, Samir Bouzbouz, Sébastien Reymond, Patrice Capdevielle, Janine Cossy.
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.Entities:
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Year: 2008 PMID： 18229938 DOI： 10.1021/jo701315h
Source DB: PubMed Journal: J Org Chem ISSN： 0022-3263 Impact factor: 4.354