A General Solution for Unstable Boronic Acids: Slow-Release Cross-Coupling from Air-Stable MIDA Boronates-Reference-Cited by-同舟云学术

A General Solution for Unstable Boronic Acids: Slow-Release Cross-Coupling from Air-Stable MIDA Boronates

Published:2009-04-30 Issue:20 Volume:131 Page:6961-6963
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Knapp David M.¹,Gillis Eric P.¹,Burke Martin D.¹

Affiliation:

1. Roger Adams Lab, Department of Chemistry, University of Illinois at Urbana−Champaign, Urbana, Illinois 61801

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja901416p

Reference65 articles.

1. Boronic Acids

2. In a recent systematic study, even the powerful diaryldialkylphosphine ligands developed by Buchwald and coworkers failed to promote efficient couplings of 2-substituted furan, thiophene, and pyrrole boronic acids with unactivated aryl chlorides:

3. Highly Efficient Monophosphine-Based Catalyst for the Palladium-Catalyzed Suzuki−Miyaura Reaction of Heteroaryl Halides and Heteroaryl Boronic Acids and Esters

4. For some examples of coupling of 2-heterocyclic boronic acids with activated aryl and acid chlorides, see:

5. aref2.

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