B(C6F5)3/CPA‐Catalyzed Aza‐Diels‐Alder Reaction of 3,3‐Difluoro‐2‐Aryl‐3H‐indoles and Unactivated Dienes

Author:

Wei Xing‐Pin1,Wang Xin‐Chun1,Ma Tao1,Qiao Xiu‐Xiu1,Li Ganpeng1,He Yonghui1,Zhao Xiao‐Jing1ORCID

Affiliation:

1. Key Laboratory of Chemistry in Ethnic Medicinal Resources Key Laboratory of Natural Products Synthetic Biology of Ethnic Medicinal Endophytes State Ethnic Affairs Commission & Ministry of Education School of Ethnic Medicine Yunnan Minzu University Kunming 650500 China

Abstract

AbstractHere we report B(C6F5)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.

Publisher

Wiley

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