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

Brett P. Fors; Donald A. Watson; Mark R. Biscoe; Stephen L. Buchwald

doi:10.1021/ja8055358

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

Journal of the American Chemical Society ◽

10.1021/ja8055358 ◽

2008 ◽

Vol 130 (41) ◽

pp. 13552-13554 ◽

Cited By ~ 372

Author(s):

Brett P. Fors ◽

Donald A. Watson ◽

Mark R. Biscoe ◽

Stephen L. Buchwald

Keyword(s):

Active Catalyst ◽

Cross Coupling ◽

Primary Amines ◽

Coupling Reactions ◽

Aryl Chlorides ◽

Cross Coupling Reactions ◽

Highly Active

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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 ◽

10.1002/chin.200907069 ◽

2009 ◽

Vol 40 (7) ◽

Author(s):

Brett P. Fors ◽

Donald A. Watson ◽

Mark R. Biscoe ◽

Stephen L. Buchwald

Keyword(s):

Active Catalyst ◽

Cross Coupling ◽

Primary Amines ◽

Coupling Reactions ◽

Aryl Chlorides ◽

Cross Coupling Reactions ◽

Highly Active

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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 ◽

Cited By ~ 633

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

ChemInform ◽

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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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

The Journal of Organic Chemistry ◽

10.1021/jo010764c ◽

2001 ◽

Vol 66 (25) ◽

pp. 8677-8681 ◽

Cited By ~ 239

Author(s):

George Y. Li ◽

Gang Zheng ◽

Andrew F. Noonan

Keyword(s):

Palladium Catalysts ◽

Cross Coupling ◽

Coupling Reactions ◽

Aryl Chlorides ◽

Cross Coupling Reactions ◽

Highly Active

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A Highly Active Catalyst for Suzuki Cross-Coupling Reactions —Pd-Cu Bimetallic Nanoparticles Supported on Graphene Nanocomposites

Studies in Synthetic Chemistry ◽

10.12677/ssc.2013.12002 ◽

2013 ◽

Vol 01 (02) ◽

pp. 5-9

Author(s):

欣燕林

Keyword(s):

Bimetallic Nanoparticles ◽

Active Catalyst ◽

Cross Coupling ◽

Coupling Reactions ◽

Graphene Nanocomposites ◽

Cross Coupling Reactions ◽

Highly Active

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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.

ChemInform ◽

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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Pd/BrettPhos: A Highly Active Catalyst for C-N Cross-Coupling Reactions

Synfacts ◽

10.1055/s-0028-1087458 ◽

2008 ◽

Vol 2009 (01) ◽

pp. 0087-0087

Keyword(s):

Active Catalyst ◽

Cross Coupling ◽

Coupling Reactions ◽

Cross Coupling Reactions ◽

Highly Active

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ChemInform Abstract: Pd-Co Bimetallic Nanoparticles Supported on Graphene as a Highly Active Catalyst for Suzuki-Miyaura and Sonogashira Cross-Coupling Reactions.

ChemInform ◽

10.1002/chin.201451055 ◽

2014 ◽

Vol 45 (51) ◽

pp. no-no

Author(s):

Yi-Si Feng ◽

Xin-Yan Lin ◽

Jian Hao ◽

Hua-Jian Xu

Keyword(s):

Bimetallic Nanoparticles ◽

Active Catalyst ◽

Cross Coupling ◽

Coupling Reactions ◽

Cross Coupling Reactions ◽

Highly Active

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A Highly Active Catalyst for Suzuki–Miyaura Cross-Coupling Reactions of Heteroaryl Compounds

Angewandte Chemie International Edition ◽

10.1002/anie.200600493 ◽

2006 ◽

Vol 45 (21) ◽

pp. 3484-3488 ◽

Cited By ~ 285

Author(s):

Kelvin L. Billingsley ◽

Kevin W. Anderson ◽

Stephen L. Buchwald

Keyword(s):

Active Catalyst ◽

Cross Coupling ◽

Coupling Reactions ◽

Cross Coupling Reactions ◽

Highly Active

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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 ◽

Cited By ~ 73

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

Download Full-text

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: 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.

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 Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated 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

A Highly Active Catalyst for Suzuki Cross-Coupling Reactions —Pd-Cu Bimetallic Nanoparticles Supported on Graphene Nanocomposites

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.

Pd/BrettPhos: A Highly Active Catalyst for C-N Cross-Coupling Reactions

ChemInform Abstract: Pd-Co Bimetallic Nanoparticles Supported on Graphene as a Highly Active Catalyst for Suzuki-Miyaura and Sonogashira Cross-Coupling Reactions.

A Highly Active Catalyst for Suzuki–Miyaura Cross-Coupling Reactions of Heteroaryl Compounds

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

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.