| Year |
Citation |
Score |
| 2021 |
Klapars A, Chung JYL, Limanto J, Calabria R, Campeau LC, Campos KR, Chen W, Dalby SM, Davis TA, DiRocco DA, Hyde AM, Kassim AM, Larsen MU, Liu G, Maligres PE, et al. Efficient synthesis of antiviral agent uprifosbuvir enabled by new synthetic methods. Chemical Science. 12: 9031-9036. PMID 34276931 DOI: 10.1039/d1sc01978c |
0.657 |
|
| 2015 |
Davis TA, Wang C, Rovis T. Rhodium(III)-Catalyzed C-H Activation: An Oxidative Intramolecular Heck-Type Reaction Directed by a Carboxylic Acid. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 26: 1520-1524. PMID 27540274 DOI: 10.1055/S-0034-1381006 |
0.6 |
|
| 2015 |
Vilgelm AE, Pawlikowski JS, Liu Y, Hawkins OE, Davis TA, Smith J, Weller KP, Horton LW, McClain CM, Ayers GD, Turner DC, Essaka DC, Stewart CF, Sosman JA, Kelley MC, et al. Mdm2 and aurora kinase a inhibitors synergize to block melanoma growth by driving apoptosis and immune clearance of tumor cells. Cancer Research. 75: 181-93. PMID 25398437 DOI: 10.1158/0008-5472.Can-14-2405 |
0.45 |
|
| 2014 |
Vara BA, Mayasundari A, Tellis JC, Danneman MW, Arredondo V, Davis TA, Min J, Finch K, Guy RK, Johnston JN. Organocatalytic, diastereo- and enantioselective synthesis of nonsymmetric cis-stilbene diamines: a platform for the preparation of single-enantiomer cis-imidazolines for protein-protein inhibition. The Journal of Organic Chemistry. 79: 6913-38. PMID 25017623 DOI: 10.1021/Jo501003R |
0.592 |
|
| 2013 |
Davis TA, Hyster TK, Rovis T. Rhodium(III)-catalyzed intramolecular hydroarylation, amidoarylation, and Heck-type reaction: three distinct pathways determined by an amide directing group. Angewandte Chemie (International Ed. in English). 52: 14181-5. PMID 24214733 DOI: 10.1002/Anie.201307631 |
0.654 |
|
| 2013 |
Davis TA, Vilgelm AE, Richmond A, Johnston JN. Preparation of (-)-Nutlin-3 using enantioselective organocatalysis at decagram scale. The Journal of Organic Chemistry. 78: 10605-16. PMID 24127627 DOI: 10.1021/Jo401321A |
0.634 |
|
| 2012 |
Davis TA, Dobish MC, Schwieter KE, Chun AC, Johnston JN. Preparation of H,(4) PyrrolidineQuin-BAM (PBAM). Organic Syntheses; An Annual Publication of Satisfactory Methods For the Preparation of Organic Chemicals. 89: 380-393. PMID 23180898 DOI: 10.15227/Orgsyn.089.0380 |
0.487 |
|
| 2012 |
Davis TA, Danneman MW, Johnston JN. Chiral proton catalysis of secondary nitroalkane additions to azomethine: synthesis of a potent GlyT1 inhibitor. Chemical Communications (Cambridge, England). 48: 5578-80. PMID 22543734 DOI: 10.1039/C2Cc32225K |
0.643 |
|
| 2011 |
Davis TA, Johnston JN. Catalytic, Enantioselective Synthesis of Stilbene cis-Diamines: A Concise Preparation of (-)-Nutlin-3, a Potent p53/MDM2 Inhibitor. Chemical Science (Royal Society of Chemistry : 2010). 2: 1076-1079. PMID 22708054 DOI: 10.1039/C1Sc00061F |
0.629 |
|
| 2011 |
Tomasiak TM, Archuleta TL, Andréll J, Luna-Chávez C, Davis TA, Sarwar M, Ham AJ, McDonald WH, Yankovskaya V, Stern HA, Johnston JN, Maklashina E, Cecchini G, Iverson TM. Geometric restraint drives on- and off-pathway catalysis by the Escherichia coli menaquinol:fumarate reductase. The Journal of Biological Chemistry. 286: 3047-56. PMID 21098488 DOI: 10.1074/Jbc.M110.192849 |
0.55 |
|
| 2010 |
Davis TA, Wilt JC, Johnston JN. Bifunctional asymmetric catalysis: amplification of Brønsted basicity can orthogonally increase the reactivity of a chiral Brønsted acid. Journal of the American Chemical Society. 132: 2880-2. PMID 20151644 DOI: 10.1021/Ja908814H |
0.664 |
|
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