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[氮杂环卡宾催化的C-C键形成及不对称反应的发展]

[Development of C-C bond formation and asymmetric reactions catalyzed by N-heterocyclic carbenes].

作者信息

Suzuki Yumiko

机构信息

School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Japan.

出版信息

Yakugaku Zasshi. 2008 Aug;128(8):1179-85. doi: 10.1248/yakushi.128.1179.

Abstract

N-Heterocyclic carbenes have been studied for their ability to catalyze C-C bond formations and asymmetric reactions. The fluoro groups of fluorobenzenes are nucleophilically substituted with aroyl groups derived from aromatic aldehydes due to the catalytic action of imidazolidenyl carbenes to afford ketones. N-Heterocyclic carbenes mediate the addition of trimethylsilyl cyanide to aldehydes to yield cyanohydrin trimethylsilyl ethers. The use of chiral imidazolidenyl carbenes derived from (R,R)-1,3-bis[(1-naphthyl)ethyl]imidazolium chloride led to enantioselective cyanosilylation. C2-symmetric imidazolidenyl carbenes catalyze the asymmetric acylation of racemic secondary alcohols.

摘要

氮杂环卡宾因其催化碳 - 碳键形成和不对称反应的能力而受到研究。由于咪唑啉亚基卡宾的催化作用,氟苯的氟基团被源自芳香醛的芳酰基亲核取代,从而得到酮。氮杂环卡宾介导三甲基硅氰化物与醛的加成反应,生成氰醇三甲基硅醚。使用由(R,R)-1,3-双[(1-萘基)乙基]咪唑鎓氯化物衍生的手性咪唑啉亚基卡宾可实现对映选择性氰基硅烷化反应。C2对称的咪唑啉亚基卡宾催化外消旋仲醇的不对称酰化反应。

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