Volume 42, Issue 9 pp. 985-989
Concise Report

Ru(II)-Catalyzed ortho C—H Allylation of N-Aryl-7-azaindoles with 2-Methylidene Cyclic Carbonate

Jing Zhang

Jing Zhang

State Key Laboratory Base of Eco-Chemical Engineering, College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao, Shandong, 266042 China

Search for more papers by this author
Quan-Jian Luo

Quan-Jian Luo

State Key Laboratory Base of Eco-Chemical Engineering, College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao, Shandong, 266042 China

Search for more papers by this author
Han-Chi Wang

Han-Chi Wang

State Key Laboratory Base of Eco-Chemical Engineering, College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao, Shandong, 266042 China

Search for more papers by this author
Jin-Heng Li

Jin-Heng Li

State Key Laboratory Base of Eco-Chemical Engineering, College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao, Shandong, 266042 China

State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou, Gansu, 730000 China

School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, Henan, 453007 China

Search for more papers by this author
Bo Sun

Corresponding Author

Bo Sun

State Key Laboratory Base of Eco-Chemical Engineering, College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao, Shandong, 266042 China

E-mail: [email protected]Search for more papers by this author
First published: 26 December 2023
Citations: 1

Comprehensive Summary

A Ru(II)-catalyzed ortho allylation reaction of N-aryl-7-azaindole with readily available 2-methylidene cyclic carbonate has been developed. This reaction is an effective pathway for synthesizing 7-azaindole derivatives with a wide scope of substrates and high yields. In addition, the method can be extended to the allylation of other heterocyclic compounds and several cyclic carbonates, highlighting the practicality of this strategy for synthesis.image

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.