Protodeboronation of Heteroaromatic, Vinyl, and Cyclopropyl Boronic Acids: pH–Rate Profiles, Autocatalysis, and Disproportionation-Reference-Cited by-同舟云学术

Protodeboronation of Heteroaromatic, Vinyl, and Cyclopropyl Boronic Acids: pH–Rate Profiles, Autocatalysis, and Disproportionation

Published:2016-07-15 Issue:29 Volume:138 Page:9145-9157
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Cox Paul A.¹,Leach Andrew G.²,Campbell Andrew D.³,Lloyd-Jones Guy C.¹

Affiliation:

1. School of Chemistry, University of Edinburgh, Joseph Black Building, David Brewster Road, Edinburgh EH9 3FJ, United Kingdom

2. School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Byrom Street, Liverpool L3 3AF, United Kingdom

3. Pharmaceutical Technology and Development, AstraZeneca, Silk Road Business Park, Macclesfield SK10 2NA, United Kingdom

Funder

European Research Council

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.6b03283

Reference85 articles.

1. Boronic Acids: Preparation and Applications in Organic Synthesis, Medicine and Materials,2nded.Hall, D., Ed;Wiley VCH:Weinheim, Germany, 2011; Vols. 1 and 2, pp1–133.

2. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides

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

4. Palladium-catalyzed cross-coupling of aryl and alkenyl boronic acids with alkenes via oxidative addition of a carbonboron bond to palladium(O)

5. New N- and O-arylations with phenylboronic acids and cupric acetate

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