Highly Reactive, Single-Component Nickel Catalyst Precursor for Suzuki-Miyuara Cross-Coupling of Heteroaryl Boronic Acids with Heteroaryl Halides

2012 ◽  
Vol 124 (51) ◽  
pp. 13009-13013 ◽  
Author(s):  
Shaozhong Ge ◽  
John F. Hartwig
Keyword(s):  
Nickel Catalyst ◽  
Cross Coupling ◽  
Boronic Acids ◽  
Single Component ◽  
Catalyst Precursor

ChemInform Abstract: Cross-Coupling of Chloroarenes with Boronic Acids Using a Water-Soluble Nickel Catalyst.

ChemInform ◽  
2010 ◽  
Vol 30 (25) ◽  
pp. no-no
Author(s):  
Jean-Christophe Galland ◽  
Monique Savignac ◽  
Jean-Pierre Genet
Keyword(s):  
Nickel Catalyst ◽  
Cross Coupling ◽  
Boronic Acids ◽  
Water Soluble

Cross-coupling of chloroarenes with boronic acids using a water-soluble nickel catalyst

1999 ◽  
Vol 40 (12) ◽  
pp. 2323-2326 ◽  
Author(s):  
Jean-Christophe Galland ◽  
Monique Savignac ◽  
Jean-Pierre Genêt
Keyword(s):  
Nickel Catalyst ◽  
Cross Coupling ◽  
Boronic Acids ◽  
Water Soluble

The Merger of CF3SO2Na and Palladium Catalysis to Enable Decarboxylative Cross-Coupling for the Synthesis of Aromatic Ketones under Room Temperature

2021 ◽  
Author(s):  
Pan Xie ◽  
Cheng Xue ◽  
Cancan Wang ◽  
Dongdong Du ◽  
Sanshan Shi
Keyword(s):  
Visible Light ◽  
Room Temperature ◽  
Palladium Catalysis ◽  
Cross Coupling ◽  
Boronic Acids ◽  
Aromatic Ketones ◽  
Aryl Ketones ◽  
Oxocarboxylic Acids

A CF3SO2Na/Pd(OAc)2 co-catalyzed strategy is developed to produce aryl ketones via visible-light-induced decarboxylative cross-coupling of α-oxocarboxylic acids and aryl boronic acids. This process was perfomed under air at room temperature,...

The Suzuki-Miyaura Cross-Coupling Reactions of 6-Halopurines with Boronic Acids Leading to 6-Aryl- and 6-Alkenylpurines

Synlett ◽  
1999 ◽  
Vol 1999 (7) ◽  
pp. 1145-1147 ◽  
Author(s):  
Martina Havelková ◽  
Michal Hocek ◽  
Michal Česnek ◽  
Dalimil Dvořák
Keyword(s):  
Cross Coupling ◽  
Boronic Acids ◽  
Coupling Reactions ◽  
Cross Coupling Reactions

scholarly journals Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)2 catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities

RSC Advances ◽  
2018 ◽  
Vol 8 (70) ◽  
pp. 40000-40015 ◽  
Author(s):  
Nedra Touj ◽  
Abdullah S. Al-Ayed ◽  
Mathieu Sauthier ◽  
Lamjed Mansour ◽  
Abdel Halim Harrath ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
Suzuki Coupling ◽  
Boronic Acids ◽  
Cytotoxic Activities ◽  
Coupling Reactions ◽  
Component System ◽  
Arylboronic Acids ◽  
Cross Coupling Reaction

The in situ prepared four component system Pd(OAc)2, 1,3-dialkylbenzimidazolium halides 2a–i and 4a–i, K2CO3 under CO atmosphere catalyses carbonylative cross-coupling reaction of 2-bromopyridine with various boronic acids to yield unsymmetrical arylpyridine ketones.

scholarly journals A convenient catalyst system for microwave accelerated cross-coupling of a range of aryl boronic acids with aryl chlorides

2007 ◽  
Vol 3 ◽  
Author(s):  
Matthew L Clarke ◽  
Marcia B France ◽  
Jose A Fuentes ◽  
Edward J Milton ◽  
Geoffrey J Roff
Keyword(s):  
Cross Coupling ◽  
Catalyst System ◽  
Boronic Acids ◽  
Aryl Chlorides
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