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Current
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Title |
Journal Link (for non-Subscribers) |
DOI Reference |
| Surry, D.S., and Buchwald, S.L. |
Diamine Ligands in Copper-Catalyzed Reactions |
Chem. Sci. |
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| Dooleweerdt, K., Fors, B.P., and Buchwald, S.L. |
Pd-Catalyzed Cross-Coupling Reactions of Amides and Aryl Mesylates |
Org. Lett. |
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| Jones, G.O., Liu, P., Houk, K.N. and Buchwald, S.L. |
Computational Explorations of Mechanisms and Ligand-Directed Selectivities of Copper-Catalyzed Ullmann-Type Reactions |
J. Am. Chem. Soc. |
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| Maiti, D. and Buchwald, S.L. |
Cu-Catalyzed Arylation of Phenols: Synthesis of Sterically Hindered and Heteroaryl Diaryl Ethers |
J. Org. Chem. |
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| Shen, X. and Buchwald, S.L. |
Rhodium-Catalyzed Asymmetric Intramolecular Hydroamination of Unactivated Alkenes |
Angew. Chem. Int. Ed. |
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| Hartman, R.L., Naber, J.R., Buchwald, S.L. and Jensen, K.F. |
Multistep Microchemical Synthesis Enabled by Microfluidic Distillation |
Angew. Chem. Int. Ed. |
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| Maiti, D. and Buchwald, S.L. |
Orthogonal Cu- and Pd-Based Catalyst Systems for the O- and N-Arylation of Aminophenols. |
J. Am. Chem. Soc. |
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| Hicks, J.D., Hyde, A.M., Cuezva, A.C., and Buchwald, S.L. |
Pd-Catalyzed N-Arylation of Secondary Acyclic Amides: Catalyst Development, Scope, and Computational Study. |
J. Am. Chem. Soc. |
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| Watson, D.A., Su, M., Teverovskiy, G., Zhang, Y., Garcia-Fortanet, J., Kinzel, T. and Buchwald, S.L. |
Formation of ArF from LPdAr(F): Catalytic Conversion of Aryl Triflates to Aryl Fluorides. |
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| Naber, J.R., Fors, B.P., Wu, X., Gunn, J.T. and Buchwald, S.L. |
Stille Cross-Coupling Reactions of Aryl Mesylates and Tosylates Using a Biarylphosphine Based Catalyst System. |
Heterocycles |
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