ChemInform Abstract: A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides.

A series of N,O-bidentate ligands were synthesized and studied as high activity ligands for palladium-catalyzed Suzuki–Miyaura cross-coupling reactions of aryl chlorides with arylboronic acids under mild conditions.

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Ligand-supported palladium-catalyzed cross-coupling reactions of (hetero) aryl chlorides

Synthetic Communications ◽

10.1080/00397911.2019.1587778 ◽

2019 ◽

Vol 49 (17) ◽

pp. 2117-2146 ◽

Cited By ~ 4

Author(s):

Efeturi Abraham Onoabedje ◽

Uchechukwu Chris Okoro

Keyword(s):

Cross Coupling ◽

Coupling Reactions ◽

Aryl Chlorides ◽

Cross Coupling Reactions ◽

Palladium Catalyzed ◽

Supported Palladium

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Triphenylphosphine as a Ligand for Room-Temperature Ni(0)-Catalyzed Cross-Coupling Reactions of Aryl Chlorides with Arylboronic Acids

The Journal of Organic Chemistry ◽

10.1021/jo052369i ◽

2006 ◽

Vol 71 (5) ◽

pp. 2167-2169 ◽

Cited By ~ 50

Author(s):

Zhen-Yu Tang ◽

Qiao-Sheng Hu

Keyword(s):

Room Temperature ◽

Cross Coupling ◽

Coupling Reactions ◽

Aryl Chlorides ◽

Arylboronic Acids ◽

Cross Coupling Reactions

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Palladium-Catalyzed Cross-Coupling Reactions of DiazineN-Oxides with Aryl Chlorides, Bromides, and Iodides

Angewandte Chemie ◽

10.1002/ange.200602773 ◽

2006 ◽

Vol 118 (46) ◽

pp. 7945-7950 ◽

Cited By ~ 60

Author(s):

Jean-Philippe Leclerc ◽

Keith Fagnou

Keyword(s):

Cross Coupling ◽

Coupling Reactions ◽

Aryl Chlorides ◽

Cross Coupling Reactions ◽

Palladium Catalyzed

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ChemInform Abstract: A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides.

A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides

ChemInform Abstract: A Highly Active Catalyst for Pd-Catalyzed Amination Reactions: Cross-Coupling Reactions Using Aryl Mesylates and the Highly Selective Monoarylation of Primary Amines Using Aryl Chlorides.

ChemInform Abstract: Highly Active, Well-Defined (Cyclopentadiene)(N-heterocyclic carbene)palladium Chloride Complexes for Room-Temperature SuzukiâMiyaura and BuchwaldâHartwig Cross-Coupling Reactions of Aryl Chlorides and Deboronation Homocoupling of Arylboronic Acids.

Highly Active, Well-Defined (Cyclopentadiene)(N-heterocyclic carbene)palladium Chloride Complexes for Room-Temperature Suzuki-Miyaura and Buchwald-Hartwig Cross-Coupling Reactions of Aryl Chlorides and Deboronation Homocoupling of Arylboronic Acids

A Highly Active Catalyst for Pd-Catalyzed Amination Reactions: Cross-Coupling Reactions Using Aryl Mesylates and the Highly Selective Monoarylation of Primary Amines Using Aryl Chlorides

Highly Active, Air-Stable Versatile Palladium Catalysts for the C−C, C−N, and C−S Bond Formations via Cross-Coupling Reactions of Aryl Chlorides

Efficient symmetrical bidentate dioxime ligand-accelerated homogeneous palladium-catalyzed Suzuki–Miyaura coupling reactions of aryl chlorides

Ligand-supported palladium-catalyzed cross-coupling reactions of (hetero) aryl chlorides

Triphenylphosphine as a Ligand for Room-Temperature Ni(0)-Catalyzed Cross-Coupling Reactions of Aryl Chlorides with Arylboronic Acids

Palladium-Catalyzed Cross-Coupling Reactions of DiazineN-Oxides with Aryl Chlorides, Bromides, and Iodides

ChemInform Abstract: Highly Active, Well-Defined (Cyclopentadiene)(N-heterocyclic carbene)palladium Chloride Complexes for Room-Temperature SuzukiâMiyaura and BuchwaldâHartwig Cross-Coupling Reactions of Aryl Chlorides and Deboronation Homocoupling of Arylboronic Acids.