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通过卡宾催化的腈形成和去对称化反应获得轴向手性芳基醛

Access to Axially Chiral Aryl Aldehydes via Carbene-Catalyzed Nitrile Formation and Desymmetrization Reaction.

作者信息

Cai Yuanlin, Lv Ya, Shu Liangzhen, Jin Zhichao, Chi Yonggui Robin, Li Tingting

机构信息

National Key Laboratory of Green Pesticide, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Guizhou University, Guiyang 550025, China.

School of Chemistry, Chemical Engineering, and Biotechnology, Nanyang Technological University, Singapore 637371, Singapore.

出版信息

Research (Wash D C). 2024 Jan 16;7:0293. doi: 10.34133/research.0293. eCollection 2024.

Abstract

An approach utilizing N-heterocyclic carbene for nitrile formation and desymmetrization reaction is developed. The process involves kinetic resolution, with the axially chiral aryl monoaldehydes obtained in moderate yields with excellent optical purities. These axially chiral aryl monoaldehydes can be conveniently transformed into functionalized molecules, showing great potential as catalysts in organic chemistry.

摘要

开发了一种利用N-杂环卡宾进行腈形成和去对称化反应的方法。该过程涉及动力学拆分,轴向手性芳基单醛以中等产率和优异的光学纯度获得。这些轴向手性芳基单醛可以方便地转化为功能化分子,在有机化学中作为催化剂显示出巨大潜力。

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