Palladium-Catalyzed Synthesis of N-Aryl Carbamates |
Vinogradova, E. V. ; Park, N. H. ; Fors, B. P. ; Buchwald, S. L. . Org. Lett. 2013, 15, 1394 - 1397. |
Palladium-catalyzed cross-coupling of aryl chlorides and triflates with sodium cyanate: a practical synthesis of unsymmetrical ureas |
Vinogradova, E. V. ; Fors, B. P. ; Buchwald, S. L. . J. Am. Chem. Soc. 2012, 134, 11132-5. |
Me3(OMe)tBuXPhos: a surrogate ligand for Me4tBuXPhos in palladium-catalyzed C-N and C-O bond-forming reactions |
Ueda, S. ; Ali, S. ; Fors, B. P. ; Buchwald, S. L. . J. Org. Chem. 2012, 77, 2543-7. |
Synthesis of Unsymmetrical Diarylureas via Pd-Catalyzed C–N Cross-Coupling Reactions |
Breitler, S. ; Oldenhuis, N. J. ; Fors, B. P. ; Buchwald, S. L. . Org. Lett. 2011, 13, 3262-3265. |
A single phosphine ligand allows palladium-catalyzed intermolecular C-O bond formation with secondary and primary alcohols |
Wu, X. ; Fors, B. P. ; Buchwald, S. L. . Angew. Chem. Int. Ed. 2011, 50, 9943-7. |
A Multiligand Based Pd Catalyst for C−N Cross-Coupling Reactions |
Fors, B. P. ; Buchwald, S. L. . J. Am. Chem. Soc. 2010, 132, 15914-15917. |
Pd-Catalyzed Cross-Coupling Reactions of Amides and Aryl Mesylates |
Dooleweerdt, K. ; Fors, B. P. ; Buchwald, S. L. . Org. Lett. 2010, 12, 2350-2353. |
Stille Cross-Coupling Reactions of Aryl Mesylates and Tosylates Using a Biarylphosphine Based Catalyst System |
Naber, J. R. ; Fors, B. P. ; Wu, X. ; Gunn, J. T. ; Buchwald, S. L. . Heterocycles 2010, 80, 1215-1226. |
Commentary on "A New, Efficient and Recyclable Lanthanum(III) Oxide-Catalyzed C-N Cross-Coupling" by S. Narayana Murthy, B. Madhav, V. Prakash Reddy, and Y. V. D. Nageswar, Adv. Synth. Catal. 2010, 352, 3241-3245 |
Fors, B. P. ; Buchwald, S. L. . Adv. Synth. Catal. 2010, 352, 3119-3120. |
An efficient system for the Pd-catalyzed cross-coupling of amides and aryl chlorides |
Fors, B. P. ; Dooleweerdt, K. ; Zeng, Q. ; Buchwald, S. L. . Tetrahedron 2009, 65, 6576-6583. |
An Efficient Process for Pd-Catalyzed C−N Cross-Coupling Reactions of Aryl Iodides: Insight Into Controlling Factors |
Fors, B. P. ; Davis, N. R. ; Buchwald, S. L. . J. Am. Chem. Soc. 2009, 131, 5766-5768. |
Pd-Catalyzed Conversion of Aryl Chlorides, Triflates, and Nonaflates to Nitroaromatics |
Fors, B. P. ; Buchwald, S. L. . J. Am. Chem. Soc. 2009, 131, 12898-12899. |
A Versatile Catalyst System for Suzuki−Miyaura Cross-Coupling Reactions of C(sp2)-Tosylates and Mesylates |
Bhayana, B. ; Fors, B. P. ; Buchwald, S. L. . Org. Lett. 2009, 11, 3954-3957. |
A New Class of Easily Activated Palladium Precatalysts for Facile C−N Cross-Coupling Reactions and the Low Temperature Oxidative Addition of Aryl Chlorides |
Biscoe, M. R. ; Fors, B. P. ; Buchwald, S. L. . J. Am. Chem. Soc. 2008, 130, 6686-6687. |
Water-Mediated Catalyst Preactivation: An Efficient Protocol for C−N Cross-Coupling Reactions |
Fors, B. P. ; Krattiger, P. ; Strieter, E. ; Buchwald, S. L. . Org. Lett. 2008, 10, 3505-3508. |
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 |
Fors, B. P. ; Watson, D. A. ; Biscoe, M. R. ; Buchwald, S. L. . J. Am. Chem. Soc. 2008, 130, 13552-13554. |
Pd-catalyzed amination reactions of aryl halides using bulky biarylmonophosphine ligands |
Altman, R. A. ; Fors, B. P. ; Buchwald, S. L. . Nature Protocols 2007, 2, 2881-2887. |