Oxygen-promoted PdCl2-catalyzed ligand-free Suzuki reaction in aqueous media
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2011/OB/C0OB00524J
Reference49 articles.
1. A General Method for the Suzuki−Miyaura Cross-Coupling of Sterically Hindered Aryl Chlorides: Synthesis of Di- and Tri-ortho-substituted Biaryls in 2-Propanol at Room Temperature
2. Palladium-Catalyzed Coupling Reactions of Aryl Chlorides
3. A Convenient Oxime-Carbapalladacycle-Catalyzed Suzuki Cross-Coupling of Aryl Chlorides in Water
4. Unparalleled Rates for the Activation of Aryl Chlorides and Bromides: Coupling with Amines and Boronic Acids in Minutes at Room Temperature
5. Take the Right Catalyst: Palladium-Catalyzed C−C, C−N, and C−O Bond Formation on Chloroarenes
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3. Anchoring of palladium onto the surface of porous MCM-41 modified with DL-pyroglutamic acid as a novel heterogeneous catalyst for Suzuki–Miyaura coupling reactions;Journal of Organometallic Chemistry;2021-11
4. Effective utilization of basic nature of WEB in copper catalyzed Chan-Lam N-arylation reaction under ligand free conditions;Current Research in Green and Sustainable Chemistry;2021
5. Palladium loaded on ZnO nanoparticles: Synthesis, characterization and application as heterogeneous catalyst for Suzuki–Miyaura cross-coupling reactions under ambient and ligand-free conditions;Materials Chemistry and Physics;2020-03
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