Molecular Design of Deep Blue Thermally Activated Delayed Fluorescence Materials Employing a Homoconjugative Triptycene Scaffold and Dihedral Angle Tuning |
Huang, W. ; Einzinger, M. ; Zhu, T. ; Chae, H. Sik; Jeon, S. ; Ihn, S. - G. ; Sim, M. ; Kim, S. ; Su, M. ; Teverovskiy, G. ; Wu, T. ; Van Voorhis, T. ; Swager, T. M. ; Baldo, M. A. ; Buchwald, S. L. . Chem. Mater. 2018, 30, 1462–1466. |
Palladium-Catalyzed Amination of Unprotected Five-Membered Heterocyclic Bromides |
Su, M. J. ; Hoshiya, N. ; Buchwald, S. L. . Org. Lett. 2014, 16, 832-835. |
Completely N1-selective palladium-catalyzed arylation of unsymmetric imidazoles: application to the synthesis of nilotinib |
Ueda, S. ; Su, M. ; Buchwald, S. L. . J. Am. Chem. Soc. 2012, 134, 700-6. |
A bulky biaryl phosphine ligand allows for palladium-catalyzed amidation of five-membered heterocycles as electrophiles |
Su, M. ; Buchwald, S. L. . Angew. Chem. Int. Ed. 2012, 51, 4710-3. |
Investigating the Dearomative Rearrangement of Biaryl Phosphine-Ligated Pd(II) Complexes |
Milner, P. J. ; Maimone, T. J. ; Su, M. ; Müller, P. ; Buchwald, S. L. . J. Am. Chem. Soc. 2012, 134, 19922 - 19934. |
Palladium(0)-catalyzed intermolecular amination of unactivated C(sp(3))-H bonds |
Pan, J. ; Su, M. ; Buchwald, S. L. . Angew. Chem. Int. Ed. 2011, 50, 8647-51. |
Highly N2-selective palladium-catalyzed arylation of 1,2,3-triazoles |
Ueda, S. ; Su, M. ; Buchwald, S. L. . Angew. Chem. Int. Ed. 2011, 50, 8944-7. |
Formation of ArF from LPdAr(F): Catalytic Conversion of Aryl Triflates to Aryl Fluorides |
Watson, D. A. ; Su, M. ; Teverovskiy, G. ; Zhang, Y. ; Garcia-Fortanet, J. ; Kinzel, T. ; Buchwald, S. L. . Science 2009, 325, 1661-1664. |