4.5 Review

Aziridine Synthesis via Nucleophilic Attack of Carbene Equivalents on Imines: the Aza-Darzens Reaction

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2009, 期 29, 页码 4911-4919

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.200900211

关键词

Nitrogen heterocycles; Carbene equivalent; Cyclization; Ylides; Asymmetric synthesis

资金

  1. Engineering and Physical Sciences Research Council (EPSRC)
  2. Royal Society
  3. Royal Society of Chemistry (RSC)
  4. AstraZeneca

向作者/读者索取更多资源

The development of new methods for the efficient synthesis of aziridines has been of considerable interest to researchers for more than 60 years, but no single method has yet emerged as uniformly applicable, especially for asymmetric synthesis of chiral aziridines. One method which has been intensely examined and expanded of late involves the nucleophilic addition to imines by anions bearing a-leaving groups; by analogy with the glycidate epoxide synthesis, these processes are often described as aza-Darzens reactions. This Microreview gives a summary of the area, with a focus on contemporary developments. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据