| An overview of N-heterocyclic carbenes MN Hopkinson, C Richter, M Schedler, F Glorius Nature 510 (7506), 485-496, 2014 | 4283 | 2014 |
| Towards mild metal-catalyzed C–H bond activation J Wencel-Delord, T Dröge, F Liu, F Glorius Chemical Society Reviews 40 (9), 4740-4761, 2011 | 2510 | 2011 |
| C–H bond activation enables the rapid construction and late-stage diversification of functional molecules J Wencel-Delord, F Glorius Nature chemistry 5 (5), 369-375, 2013 | 2290 | 2013 |
| Mild metal-catalyzed C–H activation: examples and concepts T Gensch, MN Hopkinson, F Glorius, J Wencel-Delord Chemical Society Reviews 45 (10), 2900-2936, 2016 | 1746 | 2016 |
| Beyond Directing Groups: Transition‐Metal‐Catalyzed C H Activation of Simple Arenes N Kuhl, MN Hopkinson, J Wencel‐Delord, F Glorius Angewandte Chemie International Edition 51 (41), 10236-10254, 2012 | 1640 | 2012 |
| Organocatalytic umpolung: N-heterocyclic carbenes and beyond X Bugaut, F Glorius Chemical Society Reviews 41 (9), 3511-3522, 2012 | 1398 | 2012 |
| The measure of all rings—N‐heterocyclic carbenes T Dröge, F Glorius Angewandte Chemie International Edition 49 (39), 6940-6952, 2010 | 1352 | 2010 |
| Energy transfer catalysis mediated by visible light: principles, applications, directions F Strieth-Kalthoff, MJ James, M Teders, L Pitzer, F Glorius Chemical Society Reviews 47 (19), 7190-7202, 2018 | 1067 | 2018 |
| N-heterocyclic carbenes in transition metal catalysis F Glorius, S Bellemin-Laponnaz Springer Science & Business Media, 2007 | 1003 | 2007 |
| Organocatalyzed conjugate umpolung of α, β‐unsaturated aldehydes for the synthesis of γ‐butyrolactones C Burstein, F Glorius Angewandte Chemie International Edition 43 (45), 6205-6208, 2004 | 833 | 2004 |
| Surveying sterically demanding N-heterocyclic carbene ligands with restricted flexibility for palladium-catalyzed cross-coupling reactions S Wuertz, F Glorius Accounts of chemical research 41 (11), 1523-1533, 2008 | 828 | 2008 |
| Extending NHC-catalysis: coupling aldehydes with unconventional reaction partners AT Biju, N Kuhl, F Glorius Accounts of chemical research 44 (11), 1182-1195, 2011 | 781 | 2011 |
| Asymmetric heterogeneous catalysis M Heitbaum, F Glorius, I Escher Angewandte Chemie International Edition 45 (29), 4732-4762, 2006 | 771 | 2006 |
| Rh (III)-catalyzed directed C− H olefination using an oxidizing directing group: mild, efficient, and versatile S Rakshit, C Grohmann, T Besset, F Glorius Journal of the American Chemical Society 133 (8), 2350-2353, 2011 | 761 | 2011 |
| Formal SN‐Type Reactions in Rhodium(III)‐Catalyzed CH Bond Activation N Kuhl, N Schröder, F Glorius Advanced Synthesis & Catalysis 356 (7), 1443-1460, 2014 | 746 | 2014 |
| Sterically demanding, bioxazoline-derived N-heterocyclic carbene ligands with restricted flexibility for catalysis G Altenhoff, R Goddard, CW Lehmann, F Glorius Journal of the American Chemical Society 126 (46), 15195-15201, 2004 | 681 | 2004 |
| Cp*Rh‐Catalyzed C—H Activations. Versatile Dehydrogenative Cross‐Couplings of Csp2 C—H Positions with Olefins, Alkynes, and Arenes FW Patureau, J Wencel‐Delord, F Glorius ChemInform 44 (29), no-no, 2013 | 618 | 2013 |
| A robustness screen for the rapid assessment of chemical reactions KD Collins, F Glorius Nature chemistry 5 (7), 597-601, 2013 | 601 | 2013 |
| Pyrrole Synthesis via Allylic sp3 C−H Activation of Enamines Followed by Intermolecular Coupling with Unactivated Alkynes S Rakshit, FW Patureau, F Glorius Journal of the American Chemical Society 132 (28), 9585-9587, 2010 | 598 | 2010 |
| Co(III)-Catalyzed C–H Activation/Formal SN-Type Reactions: Selective and Efficient Cyanation, Halogenation, and Allylation DG Yu, T Gensch, F de Azambuja, S Vasquez-Cespedes, F Glorius Journal of the American Chemical Society 136 (51), 17722-17725, 2014 | 557 | 2014 |
Dongbing ZhaoCollege of chemistry, Nankai UniversityBestätigte E-Mail-Adresse bei nankai.edu.cn
