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26 in total

1. Concise palladium-catalyzed synthesis of dibenzodiazepines and structural analogues.

Authors: Dmitry Tsvelikhovsky; Stephen L Buchwald
Journal: J Am Chem Soc Date: 2011-08-22 Impact factor: 15.419

2. A multiligand based Pd catalyst for C-N cross-coupling reactions.

Authors: Brett P Fors; Stephen L Buchwald
Journal: J Am Chem Soc Date: 2010-10-27 Impact factor: 15.419

3. Homogeneous catalytic hydroamination of alkynes and allenes with ammonia.

Authors: Vincent Lavallo; Guido D Frey; Bruno Donnadieu; Michele Soleilhavoup; Guy Bertrand
Journal: Angew Chem Int Ed Engl Date: 2008 Impact factor: 15.336

4. Dialkylbiaryl Phosphines in Pd-Catalyzed Amination: A User's Guide.

Authors: David S Surry; Stephen L Buchwald
Journal: Chem Sci Date: 2011 Impact factor: 9.825

Review 5. Biaryl phosphane ligands in palladium-catalyzed amination.

Authors: David S Surry; Stephen L Buchwald
Journal: Angew Chem Int Ed Engl Date: 2008 Impact factor: 15.336

6. Transitioning organic synthesis from organic solvents to water. What's your E Factor?

Authors: Bruce H Lipshutz; Subir Ghorai
Journal: Green Chem Date: 2014-08-01 Impact factor: 10.182

7. Evolution of a fourth generation catalyst for the amination and thioetherification of aryl halides.

Authors: John F Hartwig
Journal: Acc Chem Res Date: 2008-11-18 Impact factor: 22.384

8. Installation of protected ammonia equivalents onto aromatic & heteroaromatic rings in water enabled by micellar catalysis.

Authors: Nicholas A Isley; Sebastian Dobarco; Bruce H Lipshutz
Journal: Green Chem Date: 2014-01-02 Impact factor: 10.182

9. Mild and highly selective palladium-catalyzed monoarylation of ammonia enabled by the use of bulky biarylphosphine ligands and palladacycle precatalysts.

Authors: Chi Wai Cheung; David S Surry; Stephen L Buchwald
Journal: Org Lett Date: 2013-07-01 Impact factor: 6.005

Review 10. Applications of Palladium-Catalyzed C-N Cross-Coupling Reactions.

Authors: Paula Ruiz-Castillo; Stephen L Buchwald
Journal: Chem Rev Date: 2016-09-30 Impact factor: 60.622