Stereoselective Total Syntheses of (3R,5R)-Sonnerlactone and (3R,5S)-Sonnerlactone

被引：0

作者：

Ghanty, Supriya ^{[1
]}

Khan, P. Rasvan ^{[1
]}

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

机构：

[1] Indian Inst Chem Technol, Ctr Semiochem, Hyderabad 500007, Andhra Pradesh, India

来源：

NATURAL PRODUCT COMMUNICATIONS | 2017年 / 12卷 / 09期

关键词：

L-malic acid; Barbier allylation; Photochemical esterification; Ring Closing Metathesis; PHOMA-HERBARUM; NONENOLIDES; PROTOCOL;

D O I：

暂无

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

A highly convergent and concise total syntheses of (3R,5R)-Sonnerlactone and (3R,5S) Sonnerlactone from a readily available L-malic acid is described. The following series of reactions such as Barbier allylation, photochemical esterification and Ring Closing Metathesis (RCM) are utilized as key steps to accomplish their syntheses.

引用

页码：1479 / 1482

页数：4

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