| A simple graphical method to determine the order in catalyst J Burés Angewandte Chemie International Edition 55 (6), 2028-2031, 2016 | 390 | 2016 |
| Variable time normalization analysis: general graphical elucidation of reaction orders from concentration profiles J Burés Angewandte Chemie 128 (52), 16318-16321, 2016 | 350 | 2016 |
| Visual kinetic analysis CDT Nielsen, J Burés Chemical science 10 (2), 348-353, 2019 | 224 | 2019 |
| Curtin–Hammett paradigm for stereocontrol in organocatalysis by diarylprolinol ether catalysts J Burés, A Armstrong, DG Blackmond Journal of the American Chemical Society 134 (15), 6741-6750, 2012 | 170 | 2012 |
| Mechanistic rationalization of organocatalyzed conjugate addition of linear aldehydes to nitro-olefins J Burés, A Armstrong, DG Blackmond Journal of the American Chemical Society 133 (23), 8822-8825, 2011 | 168 | 2011 |
| Ag (I)-catalyzed C–H activation: The role of the Ag (I) salt in Pd/Ag-mediated C–H arylation of electron-deficient arenes D Whitaker, J Bures, I Larrosa Journal of the American Chemical Society 138 (27), 8384-8387, 2016 | 167 | 2016 |
| Intermediacy of Ni–Ni Species in sp2 C–O Bond Cleavage of Aryl Esters: Relevance in Catalytic C–Si Bond Formation RJ Somerville, LVA Hale, E Gómez-Bengoa, J Burés, R Martin Journal of the American Chemical Society 140 (28), 8771-8780, 2018 | 93 | 2018 |
| Catalytic Staudinger Vilarrasa Reaction for the Direct Ligation of Carboxylic Acids and Azides J Bures, M Martin, F Urpi, J Vilarrasa The Journal of organic chemistry 74 (5), 2203-2206, 2009 | 90 | 2009 |
| Explaining anomalies in enamine catalysis:“downstream species” as a new paradigm for stereocontrol J Burés, A Armstrong, DG Blackmond Accounts of chemical research 49 (2), 214-222, 2016 | 79 | 2016 |
| Enamine carboxylates as stereodetermining intermediates in prolinate catalysis JE Hein, J Burés, Y Lam, M Hughes, KN Houk, A Armstrong, ... Organic letters 13 (20), 5644-5647, 2011 | 73 | 2011 |
| Seebach’s oxazolidinone is a good catalyst for aldol reactions C Isart, J Burés, J Vilarrasa Tetrahedron Letters 49 (37), 5414-5418, 2008 | 72 | 2008 |
| Relative tendency of carbonyl compounds to form enamines D Sánchez, D Bastida, J Burés, C Isart, O Pineda, J Vilarrasa Organic Letters 14 (2), 536-539, 2012 | 71 | 2012 |
| Kinetic treatments for catalyst activation and deactivation processes based on variable time normalization analysis A Martínez‐Carrión, MG Howlett, C Alamillo‐Ferrer, AD Clayton, ... Angewandte Chemie International Edition 58 (30), 10189-10193, 2019 | 56 | 2019 |
| Kinetic correlation between aldehyde/enamine stereoisomers in reactions between aldehydes with α-stereocenters and chiral pyrrolidine-based catalysts J Burés, A Armstrong, DG Blackmond Chemical Science 3 (4), 1273-1277, 2012 | 54 | 2012 |
| Organic reaction mechanism classification using machine learning J Burés, I Larrosa Nature 613 (7945), 689-695, 2023 | 46 | 2023 |
| What is the Order of a Reaction? J Burés Topics in Catalysis 60, 631-633, 2017 | 44 | 2017 |
| Rationalization of an unusual solvent‐induced inversion of enantiomeric excess in organocatalytic selenylation of aldehydes J Burés, P Dingwall, A Armstrong, DG Blackmond Angewandte Chemie International Edition 53 (33), 8700-8704, 2014 | 39 | 2014 |
| Catalytic, PMe3-mediated conversion of secondary nitroalkanes to ketones: a very mild Nef-type process J Bures, J Vilarrasa Tetrahedron Letters 49 (3), 441-444, 2008 | 27 | 2008 |
| Hydroarylation of Alkenes by Protonation/Friedel–Crafts Trapping: HFIP-Mediated Access to Per-aryl Quaternary Stereocenters CDT Nielsen, AJP White, D Sale, J Bures, AC Spivey The Journal of organic chemistry 84 (22), 14965-14973, 2019 | 25 | 2019 |
| Chirality-induced catalyst aggregation: insights into catalyst speciation and activity using chiral aluminum catalysts in cyclic ester ring-opening polymerization S Gesslbauer, G Hutchinson, AJP White, J Bures, C Romain ACS Catalysis 11 (7), 4084-4093, 2021 | 24 | 2021 |
Donna G. BlackmondThe Scripps Research Institute; Imperial CollegeVerified email at scripps.edu
