Year |
Citation |
Score |
2023 |
Hendy CM, Pratt CJ, Jui NT, Blakey SB. Defluoroalkylation of Trifluoromethylarenes with Hydrazones: Rapid Access to Benzylic Difluoroarylethylamines. Organic Letters. 25: 1397-1402. PMID 36848497 DOI: 10.1021/acs.orglett.3c00126 |
0.701 |
|
2022 |
Maust MC, Hendy CM, Jui NT, Blakey SB. Switchable Regioselective 6- or 5- Radical Cyclization via Photoredox Catalysis. Journal of the American Chemical Society. PMID 35200024 DOI: 10.1021/jacs.2c00192 |
0.649 |
|
2021 |
McDaniel KA, Blood AR, Smith GC, Jui NT. Dearomatization of Unactivated Arenes via Catalytic Hydroalkylation. Acs Catalysis. 11: 4968-4972. PMID 34367722 DOI: 10.1021/acscatal.1c00732 |
0.4 |
|
2021 |
Spurlin RM, Harris AL, Pratt CJ, Jui NT. Synthesis of Spirocyclic Piperidines by Radical Hydroarylation. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 32: 211-214. PMID 34326573 DOI: 10.1055/a-1315-1014 |
0.739 |
|
2021 |
McDaniel KA, Jui NT. Dearomatization through Photoredox Hydroarylation: Discovery of a Radical-Polar Crossover Strategy. Organic Letters. 23: 5576-5580. PMID 34232663 DOI: 10.1021/acs.orglett.1c02006 |
0.439 |
|
2021 |
McDaniel KA, Jui NT. Dearomatization through Photoredox Hydroarylation: Discovery of a Radical-Polar Crossover Strategy. Organic Letters. 23: 5576-5580. PMID 34232663 DOI: 10.1021/acs.orglett.1c02006 |
0.439 |
|
2021 |
Hendy CM, Smith GC, Xu Z, Lian T, Jui NT. Radical Chain Reduction via Carbon Dioxide Radical Anion (CO). Journal of the American Chemical Society. PMID 34102836 DOI: 10.1021/jacs.1c04427 |
0.42 |
|
2020 |
Flynn AR, McDaniel K, Hughes M, Vogt D, Jui NT. Hydroarylation of Arenes via Reductive Radical-Polar Crossover. Journal of the American Chemical Society. PMID 32379445 DOI: 10.1021/jacs.0c03926 |
0.377 |
|
2020 |
Pratt CJ, Aycock RA, King MD, Jui NT. Radical α-C-H Cyclobutylation of Aniline Derivatives. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 31: 51-54. PMID 32103861 DOI: 10.1055/s-0039-1690197 |
0.734 |
|
2019 |
Seath CP, Jui NT. Intermolecular Reactions of Pyridyl Radicals with Olefins via Photoredox Catalysis. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 30: 1607-1614. PMID 31938012 DOI: 10.1055/s-0037-1611527 |
0.424 |
|
2019 |
Vogt DB, Seath CP, Wang H, Jui NT. Selective C-F Functionalization of Unactivated Trifluoromethylarenes. Journal of the American Chemical Society. PMID 31369264 DOI: 10.1021/Jacs.9B06004 |
0.425 |
|
2019 |
Boyington AJ, Seath CP, Zearfoss AM, Xu Z, Jui NT. A Catalytic Strategy for Regioselective Arylethylamine Synthesis. Journal of the American Chemical Society. PMID 30759339 DOI: 10.1021/jacs.9b01077 |
0.382 |
|
2018 |
Seath CP, Vogt DB, Xu Z, Boyington AJ, Jui NT. Radical Hydroarylation of Functionalized Olefins and Mechanistic Investigation of Photocatalytic Pyridyl Radical Reactions. Journal of the American Chemical Society. PMID 30354095 DOI: 10.1021/jacs.8b10238 |
0.41 |
|
2018 |
Aycock RA, Pratt CJ, Jui NT. Aminoalkyl Radicals as Powerful Intermediates for the Synthesis of Unnatural Amino Acids and Peptides Acs Catalysis. 8: 9115-9119. DOI: 10.1021/acscatal.8b03031 |
0.7 |
|
2017 |
Wang H, Jui NT. Catalytic Defluoroalkylation of Trifluoromethylaromatics with Unactivated Alkenes. Journal of the American Chemical Society. PMID 29256607 DOI: 10.1021/Jacs.7B12590 |
0.416 |
|
2017 |
Aycock RA, Wang H, Jui NT. A mild catalytic system for radical conjugate addition of nitrogen heterocycles. Chemical Science. 8: 3121-3125. PMID 28507687 DOI: 10.1039/C7Sc00243B |
0.397 |
|
2017 |
Boyington AJ, Riu MY, Jui NT. Anti-Markovnikov Hydroarylation of Unactivated Olefins via Pyridyl Radical Intermediates. Journal of the American Chemical Society. PMID 28472584 DOI: 10.1021/jacs.7b03262 |
0.407 |
|
2014 |
Ernst JB, Tay NE, Jui NT, Buchwald SL. Regioselective synthesis of benzimidazolones via cascade C-N coupling of monosubstituted ureas. Organic Letters. 16: 3844-6. PMID 24971635 DOI: 10.1021/Ol501531Q |
0.551 |
|
2013 |
Tardiff DF, Jui NT, Khurana V, Tambe MA, Thompson ML, Chung CY, Kamadurai HB, Kim HT, Lancaster AK, Caldwell KA, Caldwell GA, Rochet JC, Buchwald SL, Lindquist S. Yeast reveal a "druggable" Rsp5/Nedd4 network that ameliorates α-synuclein toxicity in neurons. Science (New York, N.Y.). 342: 979-83. PMID 24158909 DOI: 10.1126/Science.1245321 |
0.439 |
|
2013 |
Chung CY, Khurana V, Auluck PK, Tardiff DF, Mazzulli JR, Soldner F, Baru V, Lou Y, Freyzon Y, Cho S, Mungenast AE, Muffat J, Mitalipova M, Pluth MD, Jui NT, et al. Identification and rescue of α-synuclein toxicity in Parkinson patient-derived neurons. Science (New York, N.Y.). 342: 983-7. PMID 24158904 DOI: 10.1126/Science.1245296 |
0.4 |
|
2013 |
Jui NT, Buchwald SL. Cascade palladium catalysis: a predictable and selectable regiocontrolled synthesis of N-arylbenzimidazoles. Angewandte Chemie (International Ed. in English). 52: 11624-7. PMID 24038854 DOI: 10.1002/Anie.201306007 |
0.551 |
|
2012 |
Jui NT, Garber JA, Finelli FG, MacMillan DW. Enantioselective organo-SOMO cycloadditions: a catalytic approach to complex pyrrolidines from olefins and aldehydes. Journal of the American Chemical Society. 134: 11400-3. PMID 22764834 DOI: 10.1021/Ja305076B |
0.77 |
|
2010 |
Jui NT, Lee ECY, MacMillan DWC. Enantioselective organo-SOMO cascade cycloadditions: A rapid approach to molecular complexity from simple aldehydes and olefins Journal of the American Chemical Society. 132: 10015-10017. PMID 20593858 DOI: 10.1021/Ja104313X |
0.576 |
|
2008 |
Graham TH, Jones CM, Jui NT, MacMillan DW. Enantioselective organo-singly occupied molecular orbital catalysis: the carbo-oxidation of styrenes. Journal of the American Chemical Society. 130: 16494-5. PMID 19049447 DOI: 10.1021/Ja8075633 |
0.76 |
|
2007 |
Nasveschuk CG, Frein JD, Jui NT, Rovis T. A diastereoselective intermolecular heck reaction of 1,3-dioxepins. Organic Letters. 9: 5099-102. PMID 17958436 DOI: 10.1021/Ol702294U |
0.585 |
|
2006 |
Nasveschuk CG, Jui NT, Rovis T. A modular approach to the synthesis of 2,3,4-trisubstituted tetrahydrofurans. Chemical Communications (Cambridge, England). 3119-21. PMID 16855705 DOI: 10.1039/B605438B |
0.579 |
|
Show low-probability matches. |