B-Alkyl sp3–sp2 Suzuki–Miyaura Couplings under Mild Aqueous Micellar Conditions
Author:
Affiliation:
1. Department of Chemistry & Biochemistry, University of California, Santa Barbara, California 93106, United States
2. ACatechol, Inc., Santa Barbara, California 93103, United States
3. Novartis Pharma AG, CH-4057 Basel, Switzerland
Funder
Division of Chemistry
Novartis
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.8b00961
Reference36 articles.
1. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
2. Palladium-Catalyzed Cross-Coupling: A Historical Contextual Perspective to the 2010 Nobel Prize
3. Recent Developments in the Suzuki-Miyaura Reaction: 2010–2014
4. Selection of boron reagents for Suzuki–Miyaura coupling
5. The B-Alkyl Suzuki-Miyaura Cross-Coupling Reaction: Development, Mechanistic Study, and Applications in Natural Product Synthesis
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3. Pd nanoparticles supported in PDMAEMA-b-PLMA micelles: A superb catalytic platform for Suzuki-Miyaura cross-coupling in water;European Polymer Journal;2024-01
4. Suzuki–Miyaura cross-couplings for alkyl boron reagent: recent developments—a review;Future Journal of Pharmaceutical Sciences;2023-08-11
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