C—C (Suzuki–Miyaura)

Highly Efficient Monophosphine-Based Catalyst for the Palladium-Catalyzed Suzuki−Miyaura Reaction of Heteroaryl Halides and Heteroaryl Boronic Acids and Esters

K. Billingsley and Buchwald, S. L. “Highly Efficient Monophosphine-Based Catalyst for the Palladium-Catalyzed Suzuki−Miyaura Reaction of Heteroaryl Halides and Heteroaryl Boronic Acids and Esters”, J. Am. Chem. Soc., 2007, 129(11), 3358-3366.

Benchtop Monitoring of Reaction Progress via Visual Recognition with a Handheld UV Lamp: In Situ Monitoring of Boronic Acids in the Suzuki−Miyaura Reaction

T. E. Barder and Buchwald, S. L. “Benchtop Monitoring of Reaction Progress via Visual Recognition with a Handheld UV Lamp: In Situ Monitoring of Boronic Acids in the Suzuki−Miyaura Reaction”, Org. Lett., 2007, 9(1), 137-139.

Pd-catalyzed Suzuki–Miyaura reactions of aryl halides using bulky biarylmonophosphine ligands

R. A. Altman and Buchwald, S. L. “Pd-catalyzed Suzuki–Miyaura reactions of aryl halides using bulky biarylmonophosphine ligands”, Nature Protocols, 2007, 2(12), 3115-3121.

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

K. L. Billingsley, Anderson, K. W. , and Buchwald, S. L. “A Highly Active Catalyst for Suzuki–Miyaura Cross-Coupling Reactions of Heteroaryl Compounds”, Angew. Chem. Int. Ed., 2006, 45(21), 3484-3488.

Catalysts for Suzuki−Miyaura Coupling Processes: Scope and Studies of the Effect of Ligand Structure

T. E. Barder, Walker, S. D. , Martinelli, J. R. , and Buchwald, S. L. “Catalysts for Suzuki−Miyaura Coupling Processes: Scope and Studies of the Effect of Ligand Structure”, J. Am. Chem. Soc., 2005, 127(13), 4685-4696.

General Catalysts for the Suzuki-Miyaura and Sonogashira Coupling Reactions of Aryl Chlorides and for the Coupling of Challenging Substrate Combinations in Water

K. W. Anderson and Buchwald, S. L. “General Catalysts for the Suzuki-Miyaura and Sonogashira Coupling Reactions of Aryl Chlorides and for the Coupling of Challenging Substrate Combinations in Water”, Angew. Chem. Int. Ed., 2005, 44(38), 6173-6177.

A Rationally Designed Universal Catalyst for Suzuki–Miyaura Coupling Processes

S. D. Walker, Barder, T. E. , Martinelli, J. R. , and Buchwald, S. L. “A Rationally Designed Universal Catalyst for Suzuki–Miyaura Coupling Processes”, Angew. Chem. Int. Ed., 2004, 43(14), 1871-1876.

Efficient Catalyst for the Suzuki−Miyaura Coupling of Potassium Aryl Trifluoroborates with Aryl Chlorides

T. E. Barder and Buchwald, S. L. “Efficient Catalyst for the Suzuki−Miyaura Coupling of Potassium Aryl Trifluoroborates with Aryl Chlorides”, Org. Lett., 2004, 6(16), 2649-2652.

The First General Palladium Catalyst for the Suzuki−Miyaura and Carbonyl Enolate Coupling of Aryl Arenesulfonates

H. Nho Nguyen, Huang, X. , and Buchwald, S. L. “The First General Palladium Catalyst for the Suzuki−Miyaura and Carbonyl Enolate Coupling of Aryl Arenesulfonates”, J. Am. Chem. Soc., 2003, 125(39), 11818-11819.

Use of Polymer-Supported Dialkylphosphinobiphenyl Ligands for Palladium-Catalyzed Amination and Suzuki Reactions

C. A. Parrish and Buchwald, S. L. “Use of Polymer-Supported Dialkylphosphinobiphenyl Ligands for Palladium-Catalyzed Amination and Suzuki Reactions”, J. Org. Chem., 2001, 66(11), 3820-3827.

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