Formal total synthesis of (+)-didemniserinolipid B

被引：14

作者：

Prasad, Kavirayani R. ^{[1
]}

Gandi, Vasudeva Rao ^{[1
]}

机构：

[1] Indian Inst Sci, Dept Organ Chem, Bangalore 560012, Karnataka, India

来源：

TETRAHEDRON-ASYMMETRY | 2010年 / 21卷 / 23期

关键词：

STEREOSELECTIVE TOTAL-SYNTHESIS; ACID;

D O I：

10.1016/j.tetasy.2010.11.006

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The formal total synthesis of (+)-didemniserinolipid B, a marine tunicate possessing a 6,8-dioxabicyclo[3.2.1]octane framework, was accomplished starting from L-(+)-tartaric acid. The key transformations in the synthesis include the elaboration of a gamma-hydroxy-amide readily obtained by desymmetrization of tartaric acid bis-amide via the controlled addition of a Grignard reagent followed by stereoselective reduction of the resulting ketone. (C) 2010 Elsevier Ltd. All rights reserved.

引用

页码：2848 / 2852

页数：5

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