| Metal–organic framework materials as catalysts JY Lee, OK Farha, J Roberts, KA Scheidt, SBT Nguyen, JT Hupp Chemical Society Reviews 38 (5), 1450-1459, 2009 | 8754 | 2009 |
| Pyrrolidinyl‐spirooxindole natural products as inspirations for the development of potential therapeutic agents CV Galliford, KA Scheidt Angewandte Chemie International Edition 46 (46), 8748-8758, 2007 | 2563 | 2007 |
| A facile synthesis of UiO-66, UiO-67 and their derivatives MJ Katz, ZJ Brown, YJ Colón, PW Siu, KA Scheidt, RQ Snurr, JT Hupp, ... Chemical Communications 49 (82), 9449-9451, 2013 | 1735 | 2013 |
| A frequency domain existence proof of single-molecule surface-enhanced Raman spectroscopy JA Dieringer, RB Lettan, KA Scheidt, RP Van Duyne Journal of the American Chemical Society 129 (51), 16249-16256, 2007 | 645 | 2007 |
| A Continuum of Progress: Applications of N‐Hetereocyclic Carbene Catalysis in Total Synthesis J Izquierdo, GE Hutson, DT Cohen, KA Scheidt Angewandte Chemie International Edition 51 (47), 11686-11698, 2012 | 519 | 2012 |
| Cooperative catalysis and activation with N‐heterocyclic carbenes MH Wang, KA Scheidt Angewandte Chemie International Edition 55 (48), 14912-14922, 2016 | 481 | 2016 |
| Natürliche pyrrolidinylspirooxindole als vorlagen für die entwicklung medizinischer wirkstoffe CV Galliford, KA Scheidt Angewandte Chemie 119 (46), 8902-8912, 2007 | 480 | 2007 |
| Single-molecule surface-enhanced Raman spectroscopy of crystal violet isotopologues: theory and experiment SL Kleinman, E Ringe, N Valley, KL Wustholz, E Phillips, KA Scheidt, ... Journal of the American Chemical Society 133 (11), 4115-4122, 2011 | 476 | 2011 |
| Cooperative Lewis acid/N-heterocyclic carbene catalysis DT Cohen, KA Scheidt Chemical science 3 (1), 53-57, 2012 | 460 | 2012 |
| Conversion of α, β-unsaturated aldehydes into saturated esters: an umpolung reaction catalyzed by nucleophilic carbenes A Chan, KA Scheidt Organic Letters 7 (5), 905-908, 2005 | 432 | 2005 |
| Cooperative catalysis by carbenes and Lewis acids in a highly stereoselective route to γ-lactams DEA Raup, B Cardinal-David, D Holte, KA Scheidt Nature chemistry 2 (9), 766-771, 2010 | 388 | 2010 |
| A dual Lewis base activation strategy for enantioselective carbene-catalyzed annulations J Izquierdo, A Orue, KA Scheidt Journal of the American Chemical Society 135 (29), 10634-10637, 2013 | 347 | 2013 |
| Catalytic enantioselective synthesis of flavanones and chromanones MM Biddle, M Lin, KA Scheidt Journal of the American Chemical Society 129 (13), 3830-3831, 2007 | 342 | 2007 |
| Highly Stereoselective Formal [3 + 3] Cycloaddition of Enals and Azomethine Imines Catalyzed by N-Heterocyclic Carbenes A Chan, KA Scheidt Journal of the American Chemical Society 129 (17), 5334-5335, 2007 | 336 | 2007 |
| Urea metal–organic frameworks as effective and size-selective hydrogen-bond catalysts JM Roberts, BM Fini, AA Sarjeant, OK Farha, JT Hupp, KA Scheidt Journal of the American Chemical Society 134 (7), 3334-3337, 2012 | 335 | 2012 |
| Discovering new reactions with N-heterocyclic carbene catalysis EM Phillips, A Chan, KA Scheidt Aldrichimica Acta 42 (3), 55, 2009 | 333 | 2009 |
| Cooperative N-Heterocyclic Carbene/Lewis Acid Catalysis for Highly Stereoselective Annulation Reactions with Homoenolates B Cardinal-David, DEA Raup, KA Scheidt Journal of the American Chemical Society 132 (15), 5345-5347, 2010 | 313 | 2010 |
| Single-molecule tip-enhanced Raman spectroscopy MD Sonntag, JM Klingsporn, LK Garibay, JM Roberts, JA Dieringer, ... The Journal of Physical Chemistry C 116 (1), 478-483, 2012 | 306 | 2012 |
| Tandem oxidation of allylic and benzylic alcohols to esters catalyzed by N-heterocyclic carbenes BE Maki, A Chan, EM Phillips, KA Scheidt Organic Letters 9 (2), 371-374, 2007 | 306 | 2007 |
| Enantioselective Friedel− Crafts alkylations catalyzed by bis (oxazolinyl) pyridine− Scandium (III) triflate complexes DA Evans, KR Fandrick, HJ Song, KA Scheidt, R Xu Journal of the American Chemical Society 129 (32), 10029-10041, 2007 | 303 | 2007 |
Joseph HuppNorthwestern University and Argonne National LaboratoryDirección de correo verificada de northwestern.edu