Rhodium(III‐Catalyzed C8‐Selective C−H Alkenylation and Alkylation of 1, 2, 3, 4‐Tetrahydroquinolines with Styrenes and Allylic Alcohols

Author:

Yang Ji1,Chen Changjun1,Zhao Haoqiang12,Li Bohan1,He Zhenni1,Xu Lijin1ORCID,Shi Qian3

Affiliation:

1. Department of chemistry Renmin University of China Beijing 100872 People's Republic of China

2. School of Chinese Materia Medica Beijing University of Chinese Medicine Beijing 100029 People's Republic of China

3. College of Chemistry & Materials Engineering Wenzhou University Wenzhou 325035 People's Republic of China

Abstract

AbstractRh(III)‐catalyzed chelation‐assisted C8‐selective C−H alkenylation and alkylation of 1,2,3,4‐tretrahydroquinolines with styrenes and allylic alcohols have been realized. The cationic Rh(III) catalytic system in combination with a catalytic amount of copper acetate uses oxygen as the terminal oxidant and catalyzes the stereoselective C8‐alkenylation of 1,2,3,4‐tetrahydroquinolines with styrenes to give the corresponding products in 56–93% yields with wide substrate scope and broad functional group compatibility. The reaction can be scaled up. Moreover, this protocol can be extended to the C8‐alkylation of 1,2,3,4‐tetrahydroquinolines with allylic alcohols, providing access to various 8‐(3‐oxoalkyl)‐1,2,3,4‐tetrahydroquinolines in 77–90% yields. The selection of N‐directing group is essential for catalysis, and the readily installable and removable N‐(2‐pyrimidyl) group proves to be optimal choice. Preliminary mechanistic studies are performed to gain insights into the reaction mechanism.magnified image

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry

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