| Year |
Citation |
Score |
| 2024 |
Uhlenbruck BJH, Josephitis CM, de Lescure L, Paton RS, McNally A. A deconstruction-reconstruction strategy for pyrimidine diversification. Nature. PMID 38697196 DOI: 10.1038/s41586-024-07474-1 |
0.312 |
|
| 2023 |
Selingo JD, Greenwood JW, Andrews MK, Patel C, Neel AJ, Pio B, Shevlin M, Phillips EM, Maddess ML, McNally A. A General Strategy for N-(Hetero)arylpiperidine Synthesis Using Zincke Imine Intermediates. Journal of the American Chemical Society. PMID 38153812 DOI: 10.1021/jacs.3c11504 |
0.389 |
|
| 2023 |
Josephitis CM, Nguyen HMH, McNally A. Late-Stage C-H Functionalization of Azines. Chemical Reviews. PMID 37134187 DOI: 10.1021/acs.chemrev.2c00881 |
0.504 |
|
| 2022 |
Boyle BT, Levy JN, de Lescure L, Paton RS, McNally A. Halogenation of the 3-position of pyridines through Zincke imine intermediates. Science (New York, N.Y.). 378: 773-779. PMID 36395214 DOI: 10.1126/science.add8980 |
0.387 |
|
| 2021 |
Greenwood JW, Boyle BT, McNally A. Pyridylphosphonium salts as alternatives to cyanopyridines in radical-radical coupling reactions. Chemical Science. 12: 10538-10543. PMID 34447547 DOI: 10.1039/d1sc02324a |
0.346 |
|
| 2021 |
Fricke PJ, Dolewski RD, McNally A. 4-Selective Pyridine Alkylation via Wittig Olefination of Dearomatized Pyridylphosphonium Ylides. Angewandte Chemie (International Ed. in English). PMID 34343390 DOI: 10.1002/anie.202109271 |
0.342 |
|
| 2021 |
Boyle BT, Koniarczyk JL, McNally A. Facile Pyridine S Ar Reactions via -Phosphonium-Pyridinium Intermediates. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 32: 215-218. PMID 33927483 DOI: 10.1055/a-1315-1279 |
0.332 |
|
| 2021 |
Zhang X, Nottingham KG, Patel C, Alegre-Requena JV, Levy JN, Paton RS, McNally A. Phosphorus-mediated sp-sp couplings for C-H fluoroalkylation of azines. Nature. PMID 33910228 DOI: 10.1038/s41586-021-03567-3 |
0.398 |
|
| 2020 |
Levy JN, Alegre-Requena JV, Liu R, Paton RS, McNally A. Selective Halogenation of Pyridines Using Designed Phosphine Reagents. Journal of the American Chemical Society. PMID 32469220 DOI: 10.1021/Jacs.0C04674 |
0.325 |
|
| 2020 |
Boyle BT, Nottingham KG, McNally A. An Organocatalytic Mitsunobu Reaction Trends in Chemistry. 2: 174-175. DOI: 10.1016/j.trechm.2019.11.001 |
0.384 |
|
| 2019 |
Zhang X, McNally A. Cobalt-Catalyzed Alkylation of Drug-Like Molecules and Pharmaceuticals Using Heterocyclic Phosphonium Salts. Acs Catalysis. 9: 4862-4866. PMID 31656687 DOI: 10.1021/acscatal.9b00851 |
0.424 |
|
| 2019 |
Boyle BT, Hilton MC, McNally A. Nonsymmetrical Bis-Azine Biaryls from Chloroazines: A Strategy Using Phosphorus Ligand-Coupling. Journal of the American Chemical Society. PMID 31483634 DOI: 10.1021/jacs.9b08504 |
0.331 |
|
| 2018 |
Anderson RG, Jett BM, McNally A. Selective formation of heteroaryl thioethers via a phosphonium ion coupling reaction. Tetrahedron. 74: 3129-3136. PMID 30479455 DOI: 10.1016/j.tet.2017.12.040 |
0.361 |
|
| 2018 |
Hilton MC, Zhang X, Boyle BT, Alegre-Requena JV, Paton RS, McNally A. Heterobiaryl synthesis by contractive C-C coupling via P(V) intermediates. Science (New York, N.Y.). 362: 799-804. PMID 30442804 DOI: 10.1126/Science.Aas8961 |
0.346 |
|
| 2018 |
Anderson RG, Jett BM, McNally A. A Unified Approach to Couple Aromatic Heteronucleophiles to Azines and Pharmaceuticals. Angewandte Chemie (International Ed. in English). PMID 30084203 DOI: 10.1002/anie.201807322 |
0.325 |
|
| 2018 |
Patel C, Mohnike M, Hilton MC, McNally A. A Strategy to Aminate Pyridines, Diazines, and Pharmaceuticals via Heterocyclic Phosphonium Salts. Organic Letters. PMID 29664307 DOI: 10.1021/acs.orglett.8b00813 |
0.351 |
|
| 2017 |
McNally A, Dolewski R, Hilton M. 4-Selective Pyridine Functionalization Reactions via Heterocyclic Phosphonium Salts Synlett. 29: 08-14. DOI: 10.1055/s-0036-1591850 |
0.312 |
|
| 2016 |
Hilton MC, Dolewski RD, McNally A. Selective Functionalization of Pyridines via Heterocyclic Phosphonium Salts. Journal of the American Chemical Society. PMID 27731999 DOI: 10.1021/jacs.6b08662 |
0.371 |
|
| 2015 |
Chan L, McNally A, Toh QY, Mendoza A, Gaunt MJ. A counteranion triggered arylation strategy using diaryliodonium fluorides Chemical Science. 6: 1277-1281. DOI: 10.1039/c4sc02856b |
0.665 |
|
| 2014 |
McNally A, Haffemayer B, Collins BS, Gaunt MJ. Palladium-catalysed C-H activation of aliphatic amines to give strained nitrogen heterocycles. Nature. 510: 129-33. PMID 24870240 DOI: 10.1038/nature13389 |
0.702 |
|
| 2014 |
McNally A, Haffemayer B, Collins BSL, Gaunt MJ. Correction: Corrigendum: Palladium-catalysed C–H activation of aliphatic amines to give strained nitrogen heterocycles Nature. 512: 338-338. DOI: 10.1038/nature13635 |
0.626 |
|
| 2013 |
Toh QY, McNally A, Vera S, Erdmann N, Gaunt MJ. Organocatalytic C-H bond arylation of aldehydes to bis-heteroaryl ketones. Journal of the American Chemical Society. 135: 3772-5. PMID 23445238 DOI: 10.1021/ja400051d |
0.689 |
|
| 2011 |
McNally A, Prier CK, MacMillan DW. Discovery of an α-amino C-H arylation reaction using the strategy of accelerated serendipity. Science (New York, N.Y.). 334: 1114-7. PMID 22116882 DOI: 10.1126/Science.1213920 |
0.529 |
|
| 2007 |
Gaunt MJ, Johansson CC, McNally A, Vo NT. Enantioselective organocatalysis. Drug Discovery Today. 12: 8-27. PMID 17198969 DOI: 10.1016/j.drudis.2006.11.004 |
0.598 |
|
| 2006 |
McNally A, Evans B, Gaunt MJ. Organocatalytic sigmatropic reactions: development of a [2,3] Wittig rearrangement through secondary amine catalysis. Angewandte Chemie (International Ed. in English). 45: 2116-9. PMID 16496275 DOI: 10.1002/anie.200504301 |
0.671 |
|
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