Potassium Trimethylsilanolate Enables Rapid, Homogeneous Suzuki−Miyaura Cross-Coupling of Boronic Esters
Author:
Affiliation:
1. Roger Adams Laboratory, University of Illinois, 600 South Matthews Avenue, Urbana, Illinois 61801, United States
Funder
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Catalysis,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acscatal.9b04353
Reference50 articles.
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3. Blakemore, D. Suzuki–Miyaura Coupling. In Synthetic Methods in Drug Discovery; The Royal Society of Chemistry, 2016; Vol. 1, pp 1–69.
4. Lee, J. C. H.; Hall, D. G. State-of-the-Art in Metal-Catalyzed Cross-Coupling Reactions of Organoboron Compounds with Organic Electrophiles. In Metal-Catalyzed Cross-Coupling Reactions and More; deMeijere, A., Brase, S., Oestreich, M., Eds. Wiley-VCH: Weinheim, Germany, 2014; pp 65–132.
5. Air Stable, Sterically Hindered Ferrocenyl Dialkylphosphines for Palladium-Catalyzed C−C, C−N, and C−O Bond-Forming Cross-Couplings
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