| Conversion of amides to esters by the nickel-catalysed activation of amide C–N bonds L Hie, NF Fine Nathel, TK Shah, EL Baker, X Hong, YF Yang, P Liu, ... Nature 524 (7563), 79-83, 2015 | 492 | 2015 |
| Polymerizable self-assembled monolayers for use in atomic layer deposition RJ Wojtecki, NFF Nathel, EA De Silva US Patent 10,782,613, 2020 | 291 | 2020 |
| Carbonyldiimidazole-mediated Lossen rearrangement P Dubé, NFF Nathel, M Vetelino, M Couturier, CL Aboussafy, S Pichette, ... Organic Letters 11 (24), 5622-5625, 2009 | 190 | 2009 |
| Nickel-catalyzed amination of aryl carbamates and sequential site-selective cross-couplings T Mesganaw, AL Silberstein, SD Ramgren, NFF Nathel, X Hong, P Liu, ... Chemical science 2 (9), 1766-1771, 2011 | 160 | 2011 |
| Nickel‐Catalyzed Activation of Acyl C− O Bonds of Methyl Esters L Hie, NF Fine Nathel, X Hong, YF Yang, KN Houk, NK Garg Angewandte Chemie International Edition 55 (8), 2810-2814, 2016 | 158 | 2016 |
| Nickel-catalyzed amination of aryl chlorides and sulfamates in 2-methyl-THF NF Fine Nathel, J Kim, L Hie, X Jiang, NK Garg ACS catalysis 4 (9), 3289-3293, 2014 | 75 | 2014 |
| Cine substitution of arenes using the aryl carbamate as a removable directing group T Mesganaw, NF Fine Nathel, NK Garg Organic letters 14 (11), 2918-2921, 2012 | 69 | 2012 |
| Total syntheses of indolactam alkaloids (−)-indolactam V,(−)-pendolmycin,(−)-lyngbyatoxin A, and (−)-teleocidin A-2 NFF Nathel, TK Shah, SM Bronner, NK Garg Chemical science 5 (6), 2184-2190, 2014 | 64 | 2014 |
| Total syntheses of indolactam alkaloids (−)-indolactam V,(−)-pendolmycin,(−)-lyngbyatoxin A, and (−)-teleocidin A-2 NFF Nathel, TK Shah, SM Bronner, NK Garg Chemical science 5 (6), 2184-2190, 2014 | 64 | 2014 |
| Quantification of the electrophilicity of benzyne and related intermediates NF Fine Nathel, LA Morrill, H Mayr, NK Garg Journal of the American Chemical Society 138 (33), 10402-10405, 2016 | 59 | 2016 |
| Thieme Chemistry Journals Awardees–Where are they now? Efficient cross-coupling of secondary amines/azoles and activated (hetero) aryl chlorides using an air-stable DPEPhos … RS Sawatzky, MJ Ferguson, M Stradiotto Synlett 28 (13), 1586-1591, 2017 | 23 | 2017 |
| Thioesterification and selenoesterification of amides via selective N–C cleavage at room temperature: N–C (O) to S/Se–C (O) interconversion MM Rahman, G Li, M Szostak Synthesis 52 (07), 1060-1066, 2020 | 21 | 2020 |
| Additive lithography–organic monolayer patterning coupled with an area-selective deposition R Wojtecki, J Ma, I Cordova, N Arellano, K Lionti, T Magbitang, ... ACS applied materials & interfaces 13 (7), 9081-9090, 2021 | 20 | 2021 |
| Catalytic α-arylation of ketones with heteroaromatic esters R Isshiki, R Takise, K Itami, K Muto, J Yamaguchi Synlett 28 (19), 2599-2603, 2017 | 20 | 2017 |
| Palladium-Catalyzed Amination of Aryl Sulfides and Sulfoxides with Azaarylamines of Poor Nucleophilicity R Pratap, H Yorimitsu Synthesis 51 (13), 2705-2712, 2019 | 8 | 2019 |
| F, Vetelino M, Couturier M, Aboussafy CL, Pichette S, Jorgensen ML, Hardink M P Dubé, NF Nathel Org. Lett 11, 5622, 2009 | 8 | 2009 |
| A Straightforward Conversion of Activated Amides and Haloalkanes into Esters under Transition-Metal-Free Cs2CO3/DMAP Conditions J Jian, Z Wang, L Chen, Y Gu, L Miao, Y Liu, Z Zeng Synthesis 51 (21), 4078-4084, 2019 | 6 | 2019 |
| Reactive Monolayers in Directed Additive Manufacturing-Area Selective Atomic Layer Deposition RJ Wojtecki, A DeSilva, NFF Nathel, H Shobha, N Arellano, A Friz, ... Journal of Photopolymer Science and Technology 31 (3), 431-436, 2018 | 6 | 2018 |
| F, Shah TK, Baker EL, Hong X, Yang YF, Liu P, Houk KN, Garg NK L Hie, NF Nathel Nature 524, 79, 2015 | 6 | 2015 |
| Thieme Chemistry Journals Awardees–Where Are They Now? Bis (2-pyridyl) amides as Readily Cleavable Amides Under Catalytic, Neutral, and Room-Temperature Conditions S Adachi, N Kumagai, M Shibasaki Synlett 29 (03), 301-305, 2018 | 5 | 2018 |
