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A concise total synthesis of the lichen macrolide (+)-aspicilin
Christophe Dubost1, Istvan E Markó, Thomas Ryckmans
1Université Catholique de Louvain, Département de Chimie, 1 Place Louis Pasteur, B-1348 Louvain La Neuve, Belgium.
Abstract:
The total synthesis of the polyhydroxylated macrolide (+)-aspicilin 5 is described using as a key step a highly diastereoselective allylation of aldehyde 6 with the uniquely functionalized allylstannane 1. (+)-Aspicilin is obtained in 18 steps and 10% overall yield. [structure: see text]
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