Masked Ketenes as Dienophiles in the Diels-Alder Reaction

被引：8
|
作者：
Mackay, Emily G. [1 ]
Newton, Christopher G. [2 ]
机构：
[1] Westfal Wilhelms Univ, Organ Chem Inst, Corrensstr 40, D-48149 Munster, Germany
[2] Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn, Lab Asymmetr Catalysis & Synth, CH-1015 Lausanne, Switzerland
来源：
AUSTRALIAN JOURNAL OF CHEMISTRY | 2016年 / 69卷 / 12期
基金：
欧盟地平线“2020”;
关键词：
NATURAL-PRODUCTS; OPTICALLY PURE; MOLECULAR-REARRANGEMENTS; CYCLOADDITION REACTIONS; TARTARIC-ACIDS; NEF REACTION; RING-SYSTEM; EQUIVALENTS; DERIVATIVES; PLATENSIMYCIN;
D O I：
10.1071/CH16428
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
The Diels-Alder reaction is one of the most powerful, well-established, and versatile reactions in organic chemistry; however, its application in certain settings remains a challenge as a result of functional group incompatibility. In this review, we examine the methods in which masked ketenes can be employed as dienophiles, taking particular note of applications in complex settings.
引用
收藏
页码：1365 / 1374
页数：10
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