Stereoselective synthesis of C1-C9 and C9-C17 fragments of (+)-13-deoxytedanolide

被引：7

作者：

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

Reddy, N. Rami ^{[1
]}

机构：

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

来源：

TETRAHEDRON | 2010年 / 66卷 / 17期

关键词：

(+)-13-Deoxytedanolide; Cytotoxicity; Evans' aldol; Chiral auxiliary; Cross-metathesis; Yamaguchi macrolactonization; Regioselective Sharpless asymmetric dihydroxylation; 18-MEMBERED ANTITUMOR MACROLIDE; EFFICIENT SHARPLESS DIHYDROXYLATION; ASYMMETRIC DIHYDROXYLATION; ALDOL CONDENSATIONS; DIVERGENT APPROACH; PROTECTING GROUP; C-13-C23; PART; SECO-ACID; TEDANOLIDE; MYRIAPORONES;

D O I：

10.1016/j.tet.2010.01.023

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

An efficient and highly stereoselective asymmetric synthesis of C1-C9 and C9-C17 fragments of (+)-13-deoxytedanolide have been achieved. Utilization of desymmetrization technique to prepare the triol with five stereogenic centers, regioselective Sharpless asymmetric dillydroxylation, Evans' aldol reaction, chiral methylation, and Wittig olefination are highlights of the synthesis. (C) 2010 Published by Elsevier Ltd.

引用

页码：3265 / 3274

页数：10

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