| Year |
Citation |
Score |
| 2023 |
Huth SE, Stone EA, Crotti S, Miller SJ. On the Ability of the N-O Bond to Support a Stable Stereogenic Axis: Peptide-Catalyzed Atroposelective -Oxidation. The Journal of Organic Chemistry. PMID 37561942 DOI: 10.1021/acs.joc.3c01385 |
0.51 |
|
| 2021 |
Stone EA, Hosseinzadeh P, Craven TW, Robertson MJ, Han Y, Hsieh SY, Metrano AJ, Baker D, Miller SJ. Isolating Conformers to Assess Dynamics of Peptidic Catalysts Using Computationally Designed Macrocyclic Peptides. Acs Catalysis. 11: 4395-4400. PMID 34659874 DOI: 10.1021/acscatal.1c01097 |
0.744 |
|
| 2021 |
Zhang CH, Spasov KA, Reilly RA, Hollander K, Stone EA, Ippolito JA, Liosi ME, Deshmukh MG, Tirado-Rives J, Zhang S, Liang Z, Miller SJ, Isaacs F, Lindenbach BD, Anderson KS, et al. Optimization of Triarylpyridinone Inhibitors of the Main Protease of SARS-CoV-2 to Low-Nanomolar Antiviral Potency. Acs Medicinal Chemistry Letters. 12: 1325-1332. PMID 34408808 DOI: 10.1021/acsmedchemlett.1c00326 |
0.356 |
|
| 2021 |
Deshmukh MG, Ippolito JA, Zhang CH, Stone EA, Reilly RA, Miller SJ, Jorgensen WL, Anderson KS. Structure-guided design of a perampanel-derived pharmacophore targeting the SARS-CoV-2 main protease. Structure (London, England : 1993). PMID 34161756 DOI: 10.1016/j.str.2021.06.002 |
0.387 |
|
| 2021 |
Zhang CH, Stone EA, Deshmukh M, Ippolito JA, Ghahremanpour MM, Tirado-Rives J, Spasov KA, Zhang S, Takeo Y, Kudalkar SN, Liang Z, Isaacs F, Lindenbach B, Miller SJ, Anderson KS, et al. Potent Noncovalent Inhibitors of the Main Protease of SARS-CoV-2 from Molecular Sculpting of the Drug Perampanel Guided by Free Energy Perturbation Calculations. Acs Central Science. 7: 467-475. PMID 33786375 DOI: 10.1021/acscentsci.1c00039 |
0.382 |
|
| 2020 |
Metrano AJ, Chinn AJ, Shugrue CR, Stone EA, Kim B, Miller SJ. Asymmetric Catalysis Mediated by Synthetic Peptides, Version 2.0: Expansion of Scope and Mechanisms. Chemical Reviews. PMID 32969640 DOI: 10.1021/acs.chemrev.0c00523 |
0.742 |
|
| 2020 |
Stone EA, Cutrona KJ, Miller SJ. Asymmetric Catalysis Upon Helically Chiral Loratadine Analogs Unveils Enantiomer-Dependent Antihistamine Activity. Journal of the American Chemical Society. PMID 32579347 DOI: 10.1021/Jacs.0C03904 |
0.553 |
|
| 2019 |
Hsieh SY, Tang YU, Crotti S, Stone E, Miller SJ. Catalytic Enantioselective Pyridine N-Oxidation. Journal of the American Chemical Society. PMID 31656070 DOI: 10.1021/Jacs.9B10414 |
0.526 |
|
| 2019 |
Neu J, Stone E, Spies J, Storch G, Hatano AS, Mercado BQ, Miller SJ, Schmuttenmaer CA. Terahertz Spectroscopy of Tetrameric Peptides. The Journal of Physical Chemistry Letters. PMID 31039310 DOI: 10.1021/Acs.Jpclett.9B01091 |
0.52 |
|
| 2019 |
Hirsch DR, Metrano AJ, Stone EA, Storch G, Miller SJ, Murelli RP. Troponoid Atropisomerism: Studies on the Configurational Stability of Tropone-Amide Chiral Axes. Organic Letters. PMID 30869521 DOI: 10.1021/Acs.Orglett.9B00707 |
0.701 |
|
| 2019 |
Stone EA, Mercado BQ, Miller SJ. Structure and Reactivity of Highly Twisted N-Acylimidazoles. Organic Letters. PMID 30860852 DOI: 10.1021/Acs.Orglett.9B00624 |
0.434 |
|
| 2018 |
Crawford JM, Stone E, Metrano AJ, Miller SJ, Sigman MS. Parameterization and Analysis of Peptide-Based Catalysts for the At-roposelective Bromination of 3-Arylquinazolin-4(3H)-ones. Journal of the American Chemical Society. PMID 29300461 DOI: 10.1021/Jacs.7B11303 |
0.724 |
|
| 2017 |
Hurtley AE, Stone E, Metrano AJ, Miller SJ. Desymmetrization of Diarylmethylamido Bis(phenols) through Peptide-Catalyzed Bromination: Enantiodivergence as a Consequence of a 2 amu Alteration at an Achiral Residue within the Catalyst. The Journal of Organic Chemistry. PMID 29020446 DOI: 10.1021/Acs.Joc.7B02339 |
0.735 |
|
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