Regiochemical Switching in Ir-Catalyzed C–H Borylation by Altering Ligand Loadings of N,B-Type Diboron Species
Author:
Affiliation:
1. Department of Chemistry, Michigan State University, 578 South Shaw Lane, East Lansing 48824-1322, Michigan United States
Funder
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c02760
Reference26 articles.
1. Total Synthesis of (+)-Complanadine A Using an Iridium-Catalyzed Pyridine C−H Functionalization
2. Toward a Continuous-Flow Synthesis of Boscalid®
3. Total Synthesis of Synechoxanthin through Iterative Cross-Coupling
4. Mild Iridium-Catalyzed Borylation of Arenes. High Turnover Numbers, Room Temperature Reactions, and Isolation of a Potential Intermediate
5. Transition metal–catalyzed remote C─H borylation: An emerging synthetic tool
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1. The Difference in Ir-Catalyzed C(sp2)–H and C(sp3)–H Bond Activation Assisted by a Directing Group: Cyclometalation via Cis- or Trans-Chelation?;Inorganic Chemistry;2024-09-05
2. Diversification of NH‐Aryl Sulfoximines through Iridium‐Catalyzed ortho‐ and meta‐Selective C−H Borylation;Advanced Synthesis & Catalysis;2023-12-28
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