First Stereoselective Total Synthesis of (3S,7R)-De-O-methylbotryosphaeriodiplodin

被引：0

作者：

Yadav, Jhillu S. ^{[1
]}

Vani, Chitteti Divya ^{[1
]}

Chowdeswari, Mule ^{[1
]}

Ananthalakshmi, K. ^{[1
]}

Bhasker, N. ^{[1
]}

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

机构：

[1] CSIR Indian Inst Chem Technol, Nat Prod Chem, Hyderabad 500607, Telangana, India

来源：

NATURAL PRODUCT COMMUNICATIONS | 2019年 / 14卷 / 01期

关键词：

Marouka allylation; Ring-closing metathesis; Macrolactones; LASIODIPLODIN; COMPLEXES; CHAIN;

D O I：

暂无

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

A simple and highly efficient first stereoselective total synthesis of a benzofused macrocyclic lactone, (3S,7R)-de-O-methylbotryosphaeriodiplodin has been accomplished utilizing Jacobson's kinetic resolution, Marouka asymmetric allylation, Stille coupling, and ring-closing metathesis (RCM) reactions as key steps.

引用

页码：135 / 140

页数：6

共 27 条

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