Tunable Electrochemical C−N versus N−N Bond Formation of Nitrogen‐Centered Radicals Enabled by Dehydrogenative Dearomatization: Biological Applications-Reference-Cited by-同舟云学术

Tunable Electrochemical C−N versus N−N Bond Formation of Nitrogen‐Centered Radicals Enabled by Dehydrogenative Dearomatization: Biological Applications

Published:2020-04-23 Issue:28 Volume:59 Page:11583-11590
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Lv Shide¹,Han Xiaoxin¹,Wang Jian‐Yong²,Zhou Mingyang¹,Wu Yanwei¹,Ma Li¹,Niu Liwei¹,Gao Wei¹,Zhou Jianhua¹,Hu Wei¹,Cui Yuezhi¹,Chen Jianbin¹^ORCID

Affiliation:

1. Shandong Provincial Key Laboratory of Molecular Engineering School of Chemistry and Pharmaceutical Engineering Qilu University of Technology (Shandong Academy of Sciences) Jinan 250353 P. R. China

2. School of Light Industry and Engineering Qilu University of Technology (Shandong Academy of Sciences) Jinan 250353 P. R. China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Shandong Province

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.202001510

Reference128 articles.

2. Applications of Palladium-Catalyzed C–N Cross-Coupling Reactions