A C–H Borylation Approach to Suzuki–Miyaura Coupling of Typically Unstable 2–Heteroaryl and Polyfluorophenyl Boronates-Reference-Cited by-同舟云学术

A C–H Borylation Approach to Suzuki–Miyaura Coupling of Typically Unstable 2–Heteroaryl and Polyfluorophenyl Boronates

Published:2012-08-02 Issue:16 Volume:14 Page:4266-4269
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Robbins Daniel W.¹,Hartwig John F.¹

Affiliation:

1. Department of Chemistry, University of Illinois, Urbana−Champaign, Urbana, Illinois 61801, United States, and University of California, Department of Chemistry, Berkeley, California 94720, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol301570t

Reference28 articles.

1. Recent applications of the Suzuki–Miyaura cross-coupling reaction in organic synthesis

2. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds

3. Potassium Organotrifluoroborates: New Perspectives in Organic Synthesis

4. Organotrifluoroborates: Protected Boronic Acids That Expand the Versatility of the Suzuki Coupling Reaction

5. Cyclic Triolborates: Air- and Water-Stable Ate Complexes of Organoboronic Acids

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