Catalytic Enantioselective Synthesis of Planar Chiral Pillar[5]arenes via Asymmetric Sonogashira Coupling

被引:2
|
作者
Zhou, Xiao-Hua [1 ]
Zhang, Xin [1 ]
Song, Yi-Ru [1 ]
Li, Xue [1 ]
Bao, Lin-Tao [1 ]
Xu, Wei-Tao [1 ]
Wang, Xu-Qing [1 ]
Yang, Hai-Bo [1 ,2 ]
Wang, Wei [1 ]
机构
[1] East China Normal Univ, Sch Chem & Mol Engn, State Key Lab Petr Mol & Proc Engn, Shanghai Key Lab Green Chem & Chem Proc, 3663 N Zhongshan Rd, Shanghai 200062, Peoples R China
[2] East China Normal Univ, Shanghai Ctr Brain Inspired Intelligent Mat & Dev, Shanghai 200241, Peoples R China
基金
上海市自然科学基金; 中国国家自然科学基金; 国家重点研发计划;
关键词
asymmetric catalysis; macrocycles; dynamic kinetic resolution; chiral rotaxanes; circularly polarized luminescence; INVERSION; DENDRIMERS;
D O I
10.1002/anie.202415190
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
As a novel type of macrocycles with attractive planar chirality, pillar[5]arenes have gained increasing research interest over the past decades, enabling their widespread applications in diverse fields such as porous materials, molecular machines, and chiral luminescence materials. However, the catalytic methodology towards the enantioselective synthesis of planar chiral pillar[5]arenes remains elusive. Here we report a novel method for the enantioselective synthesis of planar chiral pillar[5]arenes via asymmetric Sonogashira coupling, giving access to a wide range of highly functionalized planar chiral pillar[5]arenes, including both homo- and hetero-rimmed ones, with excellent enantioselectivities. Attractively, the resultant planar chiral pillar[5]arenes show great potential for widespread use in many areas such as chiral luminescent materials. This work not only enables the successful synthesis of planar chiral pillar[5]arenes with abundant structural and functional diversity as key building blocks for practical applications but also enriches the asymmetric cross-coupling methodologies in organic synthetic chemistry.
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页数:9
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