Balancing Reactivity, Regioselectivity, and Product Stability in Ir-Catalyzed Ortho-C–H Borylations of Anilines by Modulating the Diboron Partner-Reference-Cited by-同舟云学术

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Balancing Reactivity, Regioselectivity, and Product Stability in Ir-Catalyzed Ortho-C–H Borylations of Anilines by Modulating the Diboron Partner

Published:2024-06-26 Issue:26 Volume:26 Page:5420-5424
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Montero Bastidas Jose R.¹^ORCID,Yadav Anshu¹^ORCID,Lee Seokjoo¹,Ghaffari Behnaz¹,Smith Milton R.¹^ORCID,Maleczka Robert E.¹^ORCID

Affiliation:

1. Department of Chemistry, Michigan State University, 578 South Shaw Lane, East Lansing, Michigan 48824, United States

Funder

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c01495

Reference23 articles.

1. C−H Activation for the Construction of C−B Bonds

2. Remarkably Selective Iridium Catalysts for the Elaboration of Aromatic C-H Bonds

3. A Stoichiometric Aromatic CH Borylation Catalyzed by Iridium( I )/2,2′‐Bipyridine Complexes at Room Temperature

4. Steric and Chelate Directing Effects in Aromatic Borylation

5. Mild Iridium-Catalyzed Borylation of Arenes. High Turnover Numbers, Room Temperature Reactions, and Isolation of a Potential Intermediate

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