Recent Advances in the Domino Annulation Reaction of Quinone Imines

Author:

Wang Zhen-Hua1ORCID,Fu Xiao-Hui1,Li Qun23,You Yong1,Yang Lei1,Zhao Jian-Qiang1ORCID,Zhang Yan-Ping1,Yuan Wei-Cheng1

Affiliation:

1. Innovation Research Center of Chiral Drugs, Institute for Advanced Study, Chengdu University, Chengdu 610106, China

2. School of Materials and Environmental Engineering, Chengdu Technological University, Chengdu 611730, China

3. College of Materials and Chemistry & Chemical Engineering, Chengdu University of Technology, Chengdu 610059, China

Abstract

Quinone imines are important derivatives of quinones with a wide range of applications in organic synthesis and the pharmaceutical industry. The attack of nucleophilic reagents on quinone imines tends to lead to aromatization of the quinone skeleton, resulting in both the high reactivity and the unique reactivity of quinone imines. The extreme value of quinone imines in the construction of nitrogen- or oxygen-containing heterocycles has attracted widespread attention, and remarkable advances have been reported recently. This review provides an overview of the application of quinone imines in the synthesis of cyclic compounds via the domino annulation reaction.

Funder

Natural Science Foundation of China

Sichuan Science and Technology Program

Publisher

MDPI AG

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