Amanote Research
Register
Sign In
Water-Soluble Palladacycles as Precursors to Highly Recyclable Catalysts for the Suzuki Coupling of Aryl Bromides in Aqueous Solvents
doi 10.1021/om050940y.s001
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Palladium(0)-Catalyzed Suzuki-Miyaura Cross-Coupling Reactions of Potassium Aryl- And Heteroaryltrifluoroborates With Alkenyl Bromides
Recyclable Choline Nicotinate and Ferulate Aqueous Solutions as Efficient Lignin Solvents
Polymers
Polymers
Plastics
Chemistry
Suzuki–Miyaura Cross-Coupling of Benzylic Bromides Under Microwave Conditions
Tetrahedron Letters
Organic Chemistry
Biochemistry
Drug Discovery
Robust Acenaphthoimidazolylidene Palladacycles: Highly Efficient Catalysts for the Amination of N-Heteroaryl Chlorides
Chemistry - An Asian Journal
Organic Chemistry
Biochemistry
Chemistry
Photochemical Nickel-Catalyzed Reductive Migratory Cross-Coupling of Alkyl Bromides With Aryl Bromides
Miyaura Borylations of Aryl Bromides in Water at Room Temperature
Israel Journal of Chemistry
Chemistry
Water-Soluble Pd Nanoparticles Synthesized From Ω-Carboxyl-S-Alkanethiosulfate Ligand Precursors as Unimolecular Micelle Catalysts
ACS Applied Materials & Interfaces
Medicine
Materials Science
Nanotechnology
Nanoscience
Suzuki–Miyaura Cross-Coupling of Potassium Alkoxyethyltrifluoroborates: Access to Aryl/Heteroarylethyloxy Motifs
Journal of Organic Chemistry
Organic Chemistry
Efficient Suzuki-Miyaura Coupling of (Hetero)aryl Chlorides With Thiophene- And Furanboronic Acids in Aqueous N-Butanol
