Scholay

学术搜索 · AI 审稿 · LaTeX 协作

Asymmetric Synthesis of Azahelicenes via CPA-Catalyzed Kinetic Resolution

作者:Weiming Liu, Yong-Jiu Hao, Yuan Zhang, Xiaochen Li, Shun‐Jun Ji, Zhong‐Jian Cai · 发表于:Organic Letters · 年份:2024 · DOI:10.1021/acs.orglett.4c04350 · 被引用次数:18 · 研究领域:Synthesis and Properties of Aromatic Compounds、Axial and Atropisomeric Chirality Synthesis、Advanced NMR Techniques and Applications

The azahelicenes are structurally fascinating and practically useful chiral scaffolds, but their synthesis, especially in a catalytically asymmetric manner, is rather challenging. Herein, we report a CPA-catalyzed transfer hydrogenation process, which enables a rapid kinetic resolution of aza[6]helicenes. The established strategy provides facile access to enantioenriched aza[6]helicenes and tetrahydro[6]helicenes from easily available starting materials. A gram-scale reaction and facile conversion of the helical products into a promising chiral Lewis base catalyst, a chiroptical switch material, and monophosphine ligands further highlight the potential application of this protocol.