Gold and Bismuth Trimetallic Synergistic Redox Catalysis for Non‐Directed C─H Arylation with Aryl Bismuth

Author:

Liu Duan‐Yang1,Zhou Sitian1,Tian Linhan1,Zhang Honglei12,He Wei2,Guo Kai2,Zhu Congqing1,Zhu Chengjian1,Konchenko Sergey N.3,Li Weipeng1,Xie Jin14ORCID

Affiliation:

1. State Key Laboratory of Coordination Chemistry Jiangsu Key Laboratory of Advanced Organic Materials Chemistry and Biomedicine Innovation Center (ChemBIC) School of Chemistry and Chemical Engineering Nanjing University Nanjing 210023 China

2. State Key Laboratory of Materials‐Oriented Chemical Engineering College of Biotechnology and Pharmaceutical Engineering Nanjing Tech University Nanjing 211816 China

3. Nikolaev Institute of Inorganic Chemistry SB RAS Acad. Lavrentieva Ave. 3 Novosibirsk 630090 Russia

4. State Key Laboratory of Natural Medicines China Pharmaceutical University Nanjing 211198 China

Abstract

AbstractThe influence of substituent effects plays an important role on the efficiency and regioselectivity toward C─H activation of non‐directed arenes. Here, an unprecedented trimetallic synergistic redox catalysis system has been developed to achieve a highly efficient and orthogonal C─H arylation of non‐directed arenes with aryl bismuth. Both electron‐rich and ‐deficient aryl bismuth can proceed C─H arylation readily, thus affording an elegant strategy for the synthesis of challenging electron‐rich and sterically hindered biaryls by means of gold catalysis. Mechanistic studies reveal that Bi(V) species generated in‐situ from Ar─Bi(III) and NFSI is not only an arylation reagent but also an oxidant to form a critical Au(II)─Au(II)─Bi intermediate (detected by HRMS). Interestingly, the binding Bi‐moiety can modulate the electronic and steric environment of gold center through cooperative interactions, thus promoting the intramolecular transmetallation and reductive elimination. In addition, the synthetic robustness of this protocol has been demonstrated by gram‐scale experiments and late‐stage functionalization of complex molecules.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Wiley

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