Year |
Citation |
Score |
2018 |
Huang W, Einzinger M, Zhu T, Chae HS, Jeon S, Ihn S, Sim M, Kim S, Su M, Teverovskiy G, Wu T, Van Voorhis T, Swager TM, Baldo MA, Buchwald SL. Molecular Design of Deep Blue Thermally Activated Delayed Fluorescence Materials Employing a Homoconjugative Triptycene Scaffold and Dihedral Angle Tuning Chemistry of Materials. 30: 1462-1466. DOI: 10.1021/Acs.Chemmater.7B03490 |
0.555 |
|
2014 |
Su M, Hoshiya N, Buchwald SL. Palladium-catalyzed amination of unprotected five-membered heterocyclic bromides. Organic Letters. 16: 832-5. PMID 24417224 DOI: 10.1021/Ol4035947 |
0.537 |
|
2012 |
Milner PJ, Maimone TJ, Su M, Chen J, Müller P, Buchwald SL. Investigating the dearomative rearrangement of biaryl phosphine-ligated Pd(II) complexes. Journal of the American Chemical Society. 134: 19922-34. PMID 23153301 DOI: 10.1021/Ja310351E |
0.68 |
|
2012 |
Su M, Buchwald SL. A bulky biaryl phosphine ligand allows for palladium-catalyzed amidation of five-membered heterocycles as electrophiles. Angewandte Chemie (International Ed. in English). 51: 4710-3. PMID 22473747 DOI: 10.1002/Anie.201201244 |
0.515 |
|
2012 |
Ueda S, Su M, Buchwald SL. Completely N1-selective palladium-catalyzed arylation of unsymmetric imidazoles: application to the synthesis of nilotinib. Journal of the American Chemical Society. 134: 700-6. PMID 22126442 DOI: 10.1021/Ja2102373 |
0.511 |
|
2011 |
Ueda S, Su M, Buchwald SL. Highly N2-selective palladium-catalyzed arylation of 1,2,3-triazoles. Angewandte Chemie (International Ed. in English). 50: 8944-7. PMID 21853510 DOI: 10.1002/Anie.201103882 |
0.491 |
|
2011 |
Pan J, Su M, Buchwald SL. Palladium(0)-catalyzed intermolecular amination of unactivated C(sp³)-H bonds. Angewandte Chemie (International Ed. in English). 50: 8647-51. PMID 21812078 DOI: 10.1002/Anie.201102880 |
0.423 |
|
2009 |
Watson DA, Su M, Teverovskiy G, Zhang Y, García-Fortanet J, Kinzel T, Buchwald SL. Formation of ArF from LPdAr(F): catalytic conversion of aryl triflates to aryl fluorides. Science (New York, N.Y.). 325: 1661-4. PMID 19679769 DOI: 10.1126/Science.1178239 |
0.598 |
|
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