作者:Yenamandra Venkateswarlu、Karuturi Rajesh、Vangaru Suresh、Jondoss Jon Paul Selvam、Chitturi Rao
DOI:10.1055/s-0029-1219236
日期:2010.4
efficient stereoselectivetotalsynthesis of cladospolide A, a polyketide natural product, has been achieved. The synthesis involves stereoselective zinc-mediated allylation, pivotal aldol coupling, and ring-closing metathesis. The pivotal aldol coupling is used for the first time for macrolide construction and provides an effective alternative to Yamaguchi macrolactonization. stereoselective synthesis