Total Synthesis of Xestodecalactone C from L-Malic Acid

被引：16

作者：

Yadav, J. S. ^{[1
]}

Rao, Y. Gopala ^{[1
]}

Ravindar, K. ^{[1
]}

Reddy, B. V. Subba ^{[1
]}

Narsaiah, A. V. ^{[1
]}

机构：

[1] Indian Inst Chem Technol, Div Organ Chem, Hyderabad 500607, Andhra Pradesh, India

来源：

SYNTHESIS-STUTTGART | 2009年 / 18期

关键词：

xestodecalactone C; Barbier allylation; stereoselective reduction; intramolecular Friedel-Crafts acylation; CHELATION-CONTROLLED REDUCTION; AQUEOUS-MEDIA; CURVULARIN; METABOLITES; SPOROSTATIN; LACTONE;

D O I：

10.1055/s-0029-1216938

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

An efficient total synthesis of the ten-membered macrolide, xestodecalactone C is described. The synthetic sequence uses Barbier-allylation, LiAlH(4)/Lil-mediated syn-stereoselective 1,3-asymmetric reduction, and intramolecular Friedel-Crafts acylation as key steps.

引用

页码：3157 / 3161

页数：5

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