Recent Applications of the Horner-Wadsworth-Emmons Reaction to the Synthesis of Natural Products

被引:0
|
作者
Bisceglia, Juan. A. [1 ]
Orelli, Liliana R. [1 ]
机构
[1] Univ Buenos Aires, Fac Farm & Bioquim, CONICET, Dept Quim Organ, RA-1113 Buenos Aires, DF, Argentina
关键词
Horner-Wadsworth-Emmons (HWE) reaction; Carbonyl olefinations; Stabilized phosphonate carbanions; Natural products; Total synthesis; alpha; beta-Unsaturated carbonyl compounds; STEREOSELECTIVE TOTAL-SYNTHESIS; PHOSPHINOXYDE ALS OLEFINIERUNGSREAGENZIEN; WITTIG OLEFINATION REACTION; Z-UNSATURATED ESTERS; ETHYL (DIARYLPHOSPHONO)ACETATES; PHOSPHORORGANISCHE VERBINDUNGEN; PHOSPHONATE CARBANIONS; 1ST SYNTHESIS; BREVETOXIN-A; FRAGMENT;
D O I
暂无
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The Horner-Wadsworth-Emmons reaction has evolved in the last years as one of the most powerful and reliable method for stereocontrolled olefin synthesis. The reaction has become a widespread standard tool in natural products total syntheses, providing access to relatively simple as well as highly complex synthetic targets. In this work we present the most representative applications within the field of natural product synthesis from 2000 to the present year. The examples comprise the synthesis of macrocycles, 5 to 7 membered rings, lipids and related compounds, alkaloids and cyclic ethers. They were chosen from a large amount of literature reports and illustrate the use of the HWE reaction in the synthesis and elaboration of key intermediates and in the crucial assembly of highly functionalized synthetic precursors.
引用
收藏
页码:2206 / 2230
页数:25
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