氮杂环卡宾(NHC)催化的联芳基二醛去对称化构建轴手性醛类化合物
收稿日期: 2022-03-23
修回日期: 2022-04-30
网络出版日期: 2022-05-07
基金资助
国家自然科学基金(21822103); 国家自然科学基金(21820102003); 国家自然科学基金(91956201); 高等学校学科创新引智计划(111 Program); 高等学校学科创新引智计划(B17019); 湖北省自然科学基金(2017AHB047)
N-Heterocyclic Carbene (NHC)-Catalyzed Desymmetrization of Biaryldialdehydes to Construct Axially Chiral Aldehydes
Received date: 2022-03-23
Revised date: 2022-04-30
Online published: 2022-05-07
Supported by
National Natural Science Foundation of China(21822103); National Natural Science Foundation of China(21820102003); National Natural Science Foundation of China(91956201); Program of Introducing Talents of Discipline to Universities of China(111 Program); Program of Introducing Talents of Discipline to Universities of China(B17019); Natural Science Foundation of Hubei Province(2017AHB047)
赵薇 , 刘京 , 何向奎 , 蒋豪 , 陆良秋 , 肖文精 . 氮杂环卡宾(NHC)催化的联芳基二醛去对称化构建轴手性醛类化合物[J]. 有机化学, 2022 , 42(8) : 2504 -2514 . DOI: 10.6023/cjoc202203048
In the field of asymmetric catalytic synthesis, axially chiral aldehydes are often used as precursors of organic catalysts or chiral ligands because of their unique structures. The development of synthetic methods with enantioselectivity and structural diversity has always been the interest of chemists. However, only few catalytic methods have been developed for the construction of structurally diverse axially chiral aldehydes. Herein, a N-heterocyclic carbene (NHC)-catalyzed oxidative esterification reaction to synthesize axially chiral aldehydes through desymmetrization strategy was developed. This method features mild conditions (room temperature), excellent yields and enantioselectivity, broad substrate scope and good function group tolerance (26 examples, 54%~97% yields, up to 99% ee). All the axially chiral aldehyde products have been fully characterized and the absolute configuration was established by comparing the results from known literature. This strategy provides new possibilities for the synthesis of axially chiral aldehydes and their derivatives.
Key words: axially chiral; N-heterocyclic carbene; desymmetrization
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