Wu Yingtao, Li Mingrui, Sun Jiaqiong, Zheng Guangfan, Zhang Qian
Jilin Province Key Laboratory of Organic Functional Molecular Design & Synthesis, Department of Chemistry, Northeast Normal University, Changchun, 130024, China.
School of Environment, Northeast Normal University, Changchun, 130117, China.
Angew Chem Int Ed Engl. 2022 Mar 28;61(14):e202117340. doi: 10.1002/anie.202117340. Epub 2022 Feb 15.
Axially chiral aldehydes have received increasing attention in enantioselective catalysis. However, only very few catalytic methods have been developed to construct structurally diverse axially chiral aldehydes. We herein describe an NHC-catalyzed atroposelective esterification of biaryl dialdehydes as a general and practical strategy for the construction of axially chiral aldehydes. Mechanistic studies indicate that coupling proceeds through a novel combination of NHC-catalyzed desymmetrization of the dialdehydes and kinetic resolution. This protocol features excellent enantioselectivity, mild conditions, good functional-group tolerance, and applicability to late-stage functionalization and provides a modular platform for the synthesis of axially chiral aldehydes and their derivatives.
轴手性醛在对映选择性催化中受到越来越多的关注。然而,目前仅开发了极少数用于构建结构多样的轴手性醛的催化方法。我们在此描述了一种氮杂环卡宾(NHC)催化的联芳基二醛的阻转选择性酯化反应,这是一种构建轴手性醛的通用且实用的策略。机理研究表明,该偶联反应通过NHC催化的二醛去对称化和动力学拆分的新组合进行。该方法具有出色的对映选择性、温和的条件、良好的官能团耐受性以及适用于后期官能团化的特点,并为轴手性醛及其衍生物的合成提供了一个模块化平台。