ChemInform Abstract: Palladium- and Nickel-Catalyzed Suzuki Cross-Coupling of Sterically Hindered Aryl Bromides with Phenylboronic Acid.

Clare Griffiths; Nicholas E. Leadbeater

doi:10.1002/chin.200027093

ChemInform Abstract: Palladium- and Nickel-Catalyzed Suzuki Cross-Coupling of Sterically Hindered Aryl Bromides with Phenylboronic Acid.

ChemInform ◽

10.1002/chin.200027093 ◽

2010 ◽

Vol 31 (27) ◽

pp. no-no

Author(s):

Clare Griffiths ◽

Nicholas E. Leadbeater

Keyword(s):

Phenylboronic Acid ◽

Cross Coupling ◽

Aryl Bromides ◽

Sterically Hindered

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Palladium and nickel catalysed Suzuki cross-coupling of sterically hindered aryl bromides with phenylboronic acid

Tetrahedron Letters ◽

10.1016/s0040-4039(00)00186-6 ◽

2000 ◽

Vol 41 (14) ◽

pp. 2487-2490 ◽

Cited By ~ 33

Author(s):

Clare Griffiths ◽

Nicholas E Leadbeater

Keyword(s):

Phenylboronic Acid ◽

Cross Coupling ◽

Aryl Bromides ◽

Sterically Hindered

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Highly Active Palladium Catalysts Supported by Bulky Proazaphosphatrane Ligands for Stille Cross-Coupling: Coupling of Aryl and Vinyl Chlorides, Room Temperature Coupling of Aryl Bromides, Coupling of Aryl Triflates, and Synthesis of Sterically Hindered Biaryls

ChemInform ◽

10.1002/chin.200519061 ◽

2005 ◽

Vol 36 (19) ◽

Author(s):

Weiping Su ◽

Sameer Urgaonkar ◽

Patrick A. McLaughlin ◽

John G. Verkade

Keyword(s):

Palladium Catalysts ◽

Room Temperature ◽

Cross Coupling ◽

Highly Active ◽

Aryl Bromides ◽

Sterically Hindered

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A Palladium Catalyst System for the Efficient Cross-Coupling Reaction of Aryl Bromides and Chlorides with Phenylboronic Acid: Synthesis and Biological Activity Evaluation

Molecules ◽

10.3390/molecules22030420 ◽

2017 ◽

Vol 22 (3) ◽

pp. 420 ◽

Cited By ~ 6

Author(s):

Boubakri Lamia ◽

Ahlem Chakchouk-Mtibaa ◽

Bilel Hallouma ◽

Lamjed Mansour ◽

Lotfi Mellouli ◽

...

Keyword(s):

Biological Activity ◽

Palladium Catalyst ◽

Phenylboronic Acid ◽

Coupling Reaction ◽

Cross Coupling ◽

Acid Synthesis ◽

Catalyst System ◽

Activity Evaluation ◽

Aryl Bromides ◽

Cross Coupling Reaction

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Suzuki—Miyaura Cross-Coupling Reaction of Aryl Bromides and Chlorides with Phenylboronic Acid under Aerobic Conditions Catalyzed by Palladium Complexes with Thiosemicarbazone Ligands.

ChemInform ◽

10.1002/chin.200528100 ◽

2005 ◽

Vol 36 (28) ◽

Author(s):

Ioannis D. Kostas ◽

Fotini J. Andreadaki ◽

Dimitra Kovala-Demertzi ◽

Christos Prentjas ◽

Mavroudis A. Demertzis

Keyword(s):

Phenylboronic Acid ◽

Coupling Reaction ◽

Cross Coupling ◽

Palladium Complexes ◽

Aerobic Conditions ◽

Aryl Bromides ◽

Cross Coupling Reaction

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Palladium/Phosphite Catalyst Systems for Efficient Cross Coupling of Aryl Bromides and Chlorides with Phenylboronic Acid

Chemistry - A European Journal ◽

10.1002/(sici)1521-3765(20000515)6:10<1830::aid-chem1830>3.0.co;2-8 ◽

2000 ◽

Vol 6 (10) ◽

pp. 1830-1833 ◽

Cited By ~ 100

Author(s):

Alexander Zapf ◽

Matthias Beller

Keyword(s):

Phenylboronic Acid ◽

Cross Coupling ◽

Aryl Bromides ◽

Catalyst Systems

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Suzuki–Miyaura cross-coupling reaction of aryl bromides and chlorides with phenylboronic acid under aerobic conditions catalyzed by palladium complexes with thiosemicarbazone ligands

Tetrahedron Letters ◽

10.1016/j.tetlet.2005.02.003 ◽

2005 ◽

Vol 46 (12) ◽

pp. 1967-1970 ◽

Cited By ~ 82

Author(s):

Ioannis D. Kostas ◽

Fotini J. Andreadaki ◽

Dimitra Kovala-Demertzi ◽

Christos Prentjas ◽

Mavroudis A. Demertzis

Keyword(s):

Phenylboronic Acid ◽

Coupling Reaction ◽

Cross Coupling ◽

Palladium Complexes ◽

Aerobic Conditions ◽

Aryl Bromides ◽

Cross Coupling Reaction

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Tetraphosphine/palladium-catalysed Suzuki cross-coupling with sterically hindered aryl bromides and arylboronic acids

Tetrahedron Letters ◽

10.1016/s0040-4039(01)01360-0 ◽

2001 ◽

Vol 42 (38) ◽

pp. 6667-6670 ◽

Cited By ~ 40

Author(s):

Marie Feuerstein ◽

Henri Doucet ◽

Maurice Santelli

Keyword(s):

Cross Coupling ◽

Arylboronic Acids ◽

Aryl Bromides ◽

Sterically Hindered

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Thiosemicarbazone-derivatised palladium nanoparticles as efficient catalyst for the Suzuki–Miyaura cross-coupling of aryl bromides with phenylboronic acid

Inorganica Chimica Acta ◽

10.1016/j.ica.2007.09.038 ◽

2008 ◽

Vol 361 (5) ◽

pp. 1562-1565 ◽

Cited By ~ 19

Author(s):

Dimitra Kovala-Demertzi ◽

Nikolaos Kourkoumelis ◽

Kinga Derlat ◽

Julita Michalak ◽

Fotini J. Andreadaki ◽

...

Keyword(s):

Palladium Nanoparticles ◽

Phenylboronic Acid ◽

Cross Coupling ◽

Efficient Catalyst ◽

Aryl Bromides

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Highly Active Palladium Catalysts Supported by Bulky Proazaphosphatrane Ligands for Stille Cross-Coupling: Coupling of Aryl and Vinyl Chlorides, Room Temperature Coupling of Aryl Bromides, Coupling of Aryl Triflates, and Synthesis of Sterically Hindered Biaryls

Journal of the American Chemical Society ◽

10.1021/ja0450096 ◽

2004 ◽

Vol 126 (50) ◽

pp. 16433-16439 ◽

Cited By ~ 137

Author(s):

Weiping Su ◽

Sameer Urgaonkar ◽

Patrick A. McLaughlin ◽

John G. Verkade

Keyword(s):

Palladium Catalysts ◽

Room Temperature ◽

Cross Coupling ◽

Highly Active ◽

Aryl Bromides ◽

Sterically Hindered

Download Full-text

Highly Active Palladium Catalysts Supported by Bulky Proazaphosphatrane Ligands for Stille Cross-Coupling: Coupling of Aryl and Vinyl Chlorides, Room Temperature Coupling of Aryl Bromides, Coupling of Aryl Triflates, and Synthesis of Sterically Hindered Biaryls.

ChemInform ◽

10.1002/chin.200519062 ◽

2005 ◽

Vol 36 (19) ◽

Author(s):

Weiping Su ◽

Sameer Urgaonkar ◽

Patrick A. McLaughlin ◽

John G. Verkade

Keyword(s):

Palladium Catalysts ◽

Room Temperature ◽

Cross Coupling ◽

Highly Active ◽

Aryl Bromides ◽

Sterically Hindered

Download Full-text