Jordi Bures
Cited by
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A simple graphical method to determine the order in catalyst
J Burés
Angewandte Chemie International Edition 55 (6), 2028-2031, 2016
Variable time normalization analysis: general graphical elucidation of reaction orders from concentration profiles
J Burés
Angewandte Chemie 128 (52), 16318-16321, 2016
Visual kinetic analysis
CDT Nielsen, J Burés
Chemical science 10 (2), 348-353, 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
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
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
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
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
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
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
Seebach’s oxazolidinone is a good catalyst for aldol reactions
C Isart, J Burés, J Vilarrasa
Tetrahedron Letters 49 (37), 5414-5418, 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
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
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
Organic reaction mechanism classification using machine learning
J Burés, I Larrosa
Nature 613 (7945), 689-695, 2023
What is the Order of a Reaction?
J Burés
Topics in Catalysis 60, 631-633, 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
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
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
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
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