| N-Heterocyclic carbene complexes in C–H activation reactions Q Zhao, G Meng, SP Nolan, M Szostak Chemical reviews 120 (4), 1981-2048, 2020 | 473 | 2020 |
| Cross-coupling reactions using samarium (II) iodide M Szostak, NJ Fazakerley, D Parmar, DJ Procter Chemical reviews 114 (11), 5959-6039, 2014 | 412 | 2014 |
| Well-defined palladium (II)–NHC precatalysts for cross-coupling reactions of amides and esters by selective N–C/O–C cleavage S Shi, SP Nolan, M Szostak Accounts of Chemical Research 51 (10), 2589-2599, 2018 | 332 | 2018 |
| Synthesis of Biaryls through Nickel‐Catalyzed Suzuki–Miyaura coupling of amides by carbon–nitrogen bond cleavage S Shi, G Meng, M Szostak Angewandte Chemie 128 (24), 7073-7077, 2016 | 311 | 2016 |
| Recent developments in the synthesis and reactivity of isoxazoles: metal catalysis and beyond F Hu, M Szostak Advanced Synthesis & Catalysis 357 (12), 2583-2614, 2015 | 299 | 2015 |
| Twisted amides: from obscurity to broadly useful transition‐metal‐catalyzed reactions by N− C amide bond activation C Liu, M Szostak Chemistry–A European Journal 23 (30), 7157-7173, 2017 | 296 | 2017 |
| P-doped porous carbon as metal free catalysts for selective aerobic oxidation with an unexpected mechanism MA Patel, F Luo, MR Khoshi, E Rabie, Q Zhang, CR Flach, R Mendelsohn, ... Acs Nano 10 (2), 2305-2315, 2016 | 296 | 2016 |
| General Olefin Synthesis by the Palladium‐Catalyzed Heck Reaction of Amides: Sterically Controlled Chemoselective N C Activation G Meng, M Szostak Angewandte Chemie 127 (48), 14726-14730, 2015 | 291 | 2015 |
| Sterically controlled Pd-catalyzed chemoselective ketone synthesis via N–C cleavage in twisted amides G Meng, M Szostak Organic letters 17 (17), 4364-4367, 2015 | 269 | 2015 |
| Recent developments in ruthenium-catalyzed C–H arylation: Array of mechanistic manifolds P Nareddy, F Jordan, M Szostak ACS Catalysis 7 (9), 5721-5745, 2017 | 267 | 2017 |
| Chemistry of bridged lactams and related heterocycles M Szostak, J Aube Chemical reviews 113 (8), 5701-5765, 2013 | 246 | 2013 |
| Iron‐Catalyzed Cross‐Couplings in the Synthesis of Pharmaceuticals: In Pursuit of Sustainability A Piontek, E Bisz, M Szostak Angewandte Chemie International Edition 57 (35), 11116-11128, 2018 | 235 | 2018 |
| Cross-coupling of amides by N–C bond activation G Meng, S Shi, M Szostak Synlett 27 (18), 2530-2540, 2016 | 233 | 2016 |
| Recent advances in the chemoselective reduction of functional groups mediated by samarium (II) iodide: a single electron transfer approach M Szostak, M Spain, DJ Procter Chemical Society Reviews 42 (23), 9155-9183, 2013 | 217 | 2013 |
| Highly chemoselective, transition-metal-free transamidation of unactivated amides and direct amidation of alkyl esters by N–C/O–C cleavage G Li, CL Ji, X Hong, M Szostak Journal of the American Chemical Society 141 (28), 11161-11172, 2019 | 194 | 2019 |
| Rhodium-catalyzed C–H bond functionalization with amides by double C–H/C–N bond activation G Meng, M Szostak Organic letters 18 (4), 796-799, 2016 | 193 | 2016 |
| Highly selective transition-metal-free transamidation of amides and amidation of esters at room temperature G Li, M Szostak Nature communications 9 (1), 4165, 2018 | 184 | 2018 |
| General Method for the Suzuki–Miyaura Cross-Coupling of Amides Using Commercially Available, Air- and Moisture-Stable Palladium/NHC (NHC = N-Heterocyclic … P Lei, G Meng, M Szostak Acs Catalysis 7 (3), 1960-1965, 2017 | 175 | 2017 |
| Metal-free transamidation of secondary amides via selective N–C cleavage under mild conditions Y Liu, S Shi, M Achtenhagen, R Liu, M Szostak Organic letters 19 (7), 1614-1617, 2017 | 174 | 2017 |
| Highly Chemoselective Reduction of Amides (Primary, Secondary, Tertiary) to Alcohols using SmI2/Amine/H2O under Mild Conditions M Szostak, M Spain, AJ Eberhart, DJ Procter Journal of the American Chemical Society 136 (6), 2268-2271, 2014 | 169 | 2014 |
