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B(C 6 F 5 ) 3 /CPA-Catalyzed Aza-Diels-Alder Reaction of 3,3-Difluoro-2-Aryl-3H-indoles and Unactivated Dienes.

Xing-Pin WeiXin-Chun WangTao MaXiu-Xiu QiaoGanpeng LiYonghui HeXiao-Jing Zhao
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2024)
Here we report B(C 6 F 5 ) 3/ CPA-catalyzed enantioselective aza-Diels-Alder reaction of 3,3-difluoro-2-Aryl-3H-indoles with unactivated dienes to access chiral 10,10-difluoro-tetrahydropyrido[1,2-a]indoles. This protocol allows the formation of pyrazole-based C2-quaternary indolin-3-ones with high enantioselectivities and regioselectivities. Moreover, gram-scale synthesis of the 10,10-difluoro-tetrahydropyrido[1,2-a]indole skeleton was successfully achieved without any reduction in both yield and enantioselectivity.
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