| Introduction of fluorine and fluorine‐containing functional groups T Liang, CN Neumann, T Ritter Angewandte Chemie International Edition 52 (32), 8214-8264, 2013 | 2384 | 2013 |
| A fluoride-derived electrophilic late-stage fluorination reagent for PET imaging E Lee, AS Kamlet, DC Powers, CN Neumann, GB Boursalian, T Furuya, ... Science 334 (6056), 639-642, 2011 | 504 | 2011 |
| Einführung von Fluor und fluorhaltigen funktionellen Gruppen T Liang, CN Neumann, T Ritter Angewandte Chemie 125 (32), 8372-8423, 2013 | 401 | 2013 |
| Concerted nucleophilic aromatic substitution with 19F− and 18F− CN Neumann, JM Hooker, T Ritter Nature 534 (7607), 369-373, 2016 | 270 | 2016 |
| Late-stage fluorination: fancy novelty or useful tool? CN Neumann, T Ritter Angewandte Chemie (International ed. in English) 54 (11), 3216-3221, 2015 | 261 | 2015 |
| Application of Palladium-Mediated 18F-Fluorination to PET Radiotracer Development: Overcoming Hurdles to Translation AS Kamlet, CN Neumann, E Lee, SM Carlin, CK Moseley, N Stephenson, ... PloS one 8 (3), e59187, 2013 | 119 | 2013 |
| Facile C–F bond formation through a concerted nucleophilic aromatic substitution mediated by the phenofluor reagent CN Neumann, T Ritter Accounts of Chemical Research 50 (11), 2822-2833, 2017 | 100 | 2017 |
| 18F-Deoxyfluorination of Phenols via Ru π-Complexes H Beyzavi, D Mandal, MG Strebl, CN Neumann, EM D’Amato, J Chen, ... ACS Central Science 3 (9), 944-948, 2017 | 89 | 2017 |
| Alkyl aryl ether bond formation with PhenoFluor X Shen, CN Neumann, C Kleinlein, NW Goldberg, T Ritter Angewandte Chemie International Edition 54 (19), 5662-5665, 2015 | 54 | 2015 |
| Fluorierung in späten Synthesestadien: extravagante Neuheit oder nützliches Hilfsmittel? CN Neumann, T Ritter Angewandte Chemie 11 (127), 3261-3267, 2015 | 42 | 2015 |
| New avenues in radical trifluoromethylselenylation with trifluoromethyl tolueneselenosulfonate C Ghiazza, C Monnereau, L Khrouz, M Médebielle, T Billard, A Tlili Synlett 30 (07), 777-782, 2019 | 36 | 2019 |
| Recent developments in the deoxyfluorination of alcohols and phenols: new reagents, mechanistic insights, and applications WL Hu, XG Hu, L Hunter Synthesis 49 (22), 4917-4930, 2017 | 35 | 2017 |
| Metal–organic framework-derived Guerbet catalyst effectively differentiates between ethanol and butanol CN Neumann, SJ Rozeveld, M Yu, AJ Rieth, M Dincă Journal of the American Chemical Society 141 (44), 17477-17481, 2019 | 32 | 2019 |
| Simple photo-induced trifluoromethylation of aromatic rings H Egami, Y Ito, T Ide, S Masuda, Y Hamashima Synthesis 50 (15), 2948-2953, 2018 | 30 | 2018 |
| Selective Aromatic C–H Hydroxylation Enabled by η6-Coordination to Iridium(III) EM D’Amato, CN Neumann, T Ritter Organometallics 34 (18), 4626-4631, 2015 | 21 | 2015 |
| Palladium-catalyzed synthesis of aryl and heteroaryl difluoromethylated phosphonates MV Ivanova, T Besset, X Pannecoucke, T Poisson Synthesis 50 (04), 778-784, 2018 | 20 | 2018 |
| Thiolate-Initiated Synthesis of Dibenzothiophenes from 2, 2′-Bis (methylthio)-1, 1′-Biaryl Derivatives through Cleavage of Two Carbon–Sulfur Bonds Y Masuya, Y Kawashima, T Kodama, N Chatani, M Tobisu Synlett 30 (17), 1995-1999, 2019 | 19 | 2019 |
| A concise and efficient approach to 2, 6-disubstituted 4-fluoropyrimidines from α-CF3 aryl ketones F Liu, X Zhang, Q Qian, C Yang Synthesis 52 (02), 273-280, 2020 | 18 | 2020 |
| Fluorination of organic compounds T Ritter, CN Neumann US Patent 10,759,764, 2020 | 16 | 2020 |
| One-pot Synthesis of Spiro-2H-pyrroles from N-Propargylic β-Enaminones E Karadeniz, M Zora Synlett 30 (10), 1231-1236, 2019 | 16 | 2019 |
Jacob HookerHarvard Medical SchoolVerified email at nmr.mgh.harvard.edu
