Carbonylative Suzuki Couplings of Aryl Bromides with Boronic Acid Derivatives under Base-Free Conditions-Reference-Cited by-同舟云学术

Carbonylative Suzuki Couplings of Aryl Bromides with Boronic Acid Derivatives under Base-Free Conditions

Published:2014-03-17 Issue:7 Volume:16 Page:1888-1891
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Bjerglund Klaus M.¹²,Skrydstrup Troels¹,Molander Gary A.²

Affiliation:

1. Center for Insoluble Protein Structures (inSPIN), Department of Chemistry and the Interdisciplinary Nanoscience Center (iNANO), Aarhus University, Gustav Wieds Vej 14, 8000 Aarhus C, Denmark

2. Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6323, United States

Funder

National Institutes of Health

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol5003362

Reference25 articles.

1. Palladium-catalyzed carbonylative cross-coupling of organoboranes with aryl iodides or benzyl halides in the presence of bis(acetylacetonato)zinc(II)

2. Synthesis of unsymmetrical biaryl ketones via palladium-catalyzed carbonylative cross-coupling reaction of arylboronic acids with iodoarenes

3. Palladium-catalyzed carbonylative coupling reactions between Ar–X and carbon nucleophiles

4. Suzuki-Miyaura Cross-Coupling in Acylation Reactions, Scope and Recent Developments

5. 14Carbon monoxide made simple - novel approach to the generation, utilization, and scrubbing of14carbon monoxide

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