Ferrocenylmethylphosphines as ligands for room temperature Ni(0)-catalyzed Suzuki–Miyaura cross-coupling reactions of aryl arenesulfonates and aryl chlorides

Tetrahedron Letters ◽

10.1016/j.tetlet.2006.01.145 ◽

2006 ◽

Vol 47 (14) ◽

pp. 2427-2430 ◽

Author(s):

Zhen-Yu Tang ◽

Stephen Spinella ◽

Qiao-Sheng Hu

Keyword(s):

Room Temperature ◽

Cross Coupling ◽

Coupling Reactions ◽

Aryl Chlorides ◽

Cross Coupling Reactions

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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 ◽

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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Macromolecular Effect: Synthesis of a Ferrocenylmethylphosphine-Containing Polymer as Highly Efficient Ligands for Room-Temperature Palladium(0)-Catalyzed Suzuki Cross-Coupling Reactions of Aryl Chlorides

Journal of the American Chemical Society ◽

10.1021/ja029021e ◽

2003 ◽

Vol 125 (10) ◽

pp. 2856-2857 ◽

Author(s):

Qiao-Sheng Hu ◽

Yong Lu ◽

Zhen-Yu Tang ◽

Hong-Bin Yu

Keyword(s):

Room Temperature ◽

Cross Coupling ◽

Coupling Reactions ◽

Aryl Chlorides ◽

Highly Efficient ◽

Cross Coupling Reactions

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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.

10.1002/chin.200949085 ◽

2009 ◽

Vol 40 (49) ◽

Author(s):

Zhong Jin ◽

Su-Xian Guo ◽

Xiao-Peng Gu ◽

Ling-Ling Qiu ◽

Hai-Bing Song ◽

...

Keyword(s):

Room Temperature ◽

Cross Coupling ◽

Palladium Chloride ◽

Coupling Reactions ◽

Chloride Complexes ◽

Aryl Chlorides ◽

Arylboronic Acids ◽

Cross Coupling Reactions ◽

Highly Active ◽

Palladium Chloride Complexes

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Macromolecular Effect: Synthesis of a Ferrocenylmethylphosphine-Containing Polymer as Highly Efficient Ligands for Room-Temperature Palladium(0)-Catalyzed Suzuki Cross-Coupling Reactions of Aryl Chlorides.

10.1002/chin.200328104 ◽

2003 ◽

Vol 34 (28) ◽

Author(s):

Qiao-Sheng Hu ◽

Yong Lu ◽

Zhen-Yu Tang ◽

Hong-Bin Yu

Keyword(s):

Room Temperature ◽

Cross Coupling ◽

Coupling Reactions ◽

Aryl Chlorides ◽

Highly Efficient ◽

Cross Coupling Reactions

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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

Advanced Synthesis & Catalysis ◽

10.1002/adsc.200900098 ◽

2009 ◽

Vol 351 (10) ◽

pp. 1575-1585 ◽

Author(s):

Zhong Jin ◽

Su-Xian Guo ◽

Xiao-Peng Gu ◽

Ling-Ling Qiu ◽

Hai-Bing Song ◽

...

Keyword(s):

Room Temperature ◽

Cross Coupling ◽

Palladium Chloride ◽

Coupling Reactions ◽

Chloride Complexes ◽

Aryl Chlorides ◽

Arylboronic Acids ◽

Cross Coupling Reactions ◽

Highly Active ◽

Palladium Chloride Complexes

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Ferrocenylmethylphosphines as Ligands for Room Temperature Ni(0)-Catalyzed Suzuki—Miyaura Cross-Coupling Reactions of Aryl Arenesulfonates and Aryl Chlorides.

10.1002/chin.200629075 ◽

2006 ◽

Vol 37 (29) ◽

Author(s):

Zhen-Yu Tang ◽

Stephen Spinella ◽

Qiao-Sheng Hu

Keyword(s):

Room Temperature ◽

Cross Coupling ◽

Coupling Reactions ◽

Aryl Chlorides ◽

Cross Coupling Reactions

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

Journal of the American Chemical Society ◽

10.1021/ja982250+ ◽

1998 ◽

Vol 120 (37) ◽

pp. 9722-9723 ◽

Author(s):

David W. Old ◽

John P. Wolfe ◽

Stephen L. Buchwald

Keyword(s):

Room Temperature ◽

Active Catalyst ◽

Cross Coupling ◽

Coupling Reactions ◽

Aryl Chlorides ◽

Cross Coupling Reactions ◽

Highly Active ◽

Palladium Catalyzed

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

10.1002/chin.200629076 ◽

2006 ◽

Vol 37 (29) ◽

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

10.1002/chin.199905063 ◽

2010 ◽

Vol 30 (5) ◽

pp. no-no

Author(s):

D. W. OLD ◽

J. P. WOLFE ◽

S. L. BUCHWALD

Keyword(s):

Room Temperature ◽

Active Catalyst ◽

Cross Coupling ◽

Coupling Reactions ◽

Aryl Chlorides ◽

Cross Coupling Reactions ◽

Highly Active ◽

Palladium Catalyzed

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Room-Temperature Ni(0)-Catalyzed Cross-Coupling Reactions of Aryl Arenesulfonates with Arylboronic Acids

Journal of the American Chemical Society ◽

10.1021/ja038752r ◽

2004 ◽

Vol 126 (10) ◽

pp. 3058-3059 ◽

Author(s):

Zhen-Yu Tang ◽

Qiao-Sheng Hu

Keyword(s):

Room Temperature ◽

Cross Coupling ◽

Coupling Reactions ◽

Arylboronic Acids ◽

Cross Coupling Reactions

Download Full-text