High-Turnover Aromatic C–H Borylation Catalyzed by POCOP-Type Pincer Complexes of Iridium
Author:
Affiliation:
1. Department of Chemistry, Texas A&M University, College Station, Texas 77842, United States
Funder
Division of Chemistry
Welch Foundation
Division of Human Resource Development
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.6b03656
Reference56 articles.
1. Synthesis and structures of the first transition-metal tris(boryl) complexes: iridium complexes (.eta.6-arene)Ir(BO2C6H4)3
2. Remarkably Selective Iridium Catalysts for the Elaboration of Aromatic C-H Bonds
3. Mild Iridium-Catalyzed Borylation of Arenes. High Turnover Numbers, Room Temperature Reactions, and Isolation of a Potential Intermediate
4. C−H Activation for the Construction of C−B Bonds
5. Borylation and Silylation of C–H Bonds: A Platform for Diverse C–H Bond Functionalizations
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