Jordi Burés
#123,640
Most Influential Person Now
Spanish chemist
Jordi Burés's AcademicInfluence.com Rankings
Jordi Buréschemistry Degrees
Chemistry
#4021
World Rank
#5077
Historical Rank
Organic Chemistry
#1028
World Rank
#1160
Historical Rank

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Chemistry
Jordi Burés's Degrees
- Bachelors Chemistry University of Barcelona
- Masters Chemistry University of Barcelona
- PhD Chemistry University of Barcelona
Why Is Jordi Burés Influential?
(Suggest an Edit or Addition)According to Wikipedia, Jordi Burés is a Reader in the Department of Chemistry at The University of Manchester. His research in general is on the areas of organic and physical chemistry, specializing in Mechanistic Studies, nuclear magnetic resonance and catalysis.
Jordi Burés's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- A Simple Graphical Method to Determine the Order in Catalyst (2016) (229)
- Variable Time Normalization Analysis: General Graphical Elucidation of Reaction Orders from Concentration Profiles. (2016) (187)
- Mechanistic rationalization of organocatalyzed conjugate addition of linear aldehydes to nitro-olefins. (2011) (121)
- Curtin-Hammett paradigm for stereocontrol in organocatalysis by diarylprolinol ether catalysts. (2012) (120)
- Ag(I)-Catalyzed C-H Activation: The Role of the Ag(I) Salt in Pd/Ag-Mediated C-H Arylation of Electron-Deficient Arenes. (2016) (90)
- Intermediacy of Ni-Ni Species in sp2 C-O Bond Cleavage of Aryl Esters: Relevance in Catalytic C-Si Bond Formation. (2018) (67)
- Catalytic Staudinger-Vilarrasa reaction for the direct ligation of carboxylic acids and azides. (2009) (57)
- Visual kinetic analysis† †Electronic supplementary information (ESI) available: Microsoft Excel files with tutorials for VTNA and RPKA and a video available at https://youtu.be/5ORFRB4U10s. See DOI: 10.1039/c8sc04698k (2018) (54)
- Explaining Anomalies in Enamine Catalysis: "Downstream Species" as a New Paradigm for Stereocontrol. (2016) (51)
- Enamine carboxylates as stereodetermining intermediates in prolinate catalysis. (2011) (48)
- Seebach’s oxazolidinone is a good catalyst for aldol reactions (2008) (46)
- A Simple Graphical Method to Determine the Order of a Reaction in Catalyst (2016) (43)
- Relative tendency of carbonyl compounds to form enamines. (2012) (40)
- Kinetic correlation between aldehyde/enamine stereoisomers in reactions between aldehydes with α-stereocenters and chiral pyrrolidine-based catalysts (2012) (36)
- Rationalization of an unusual solvent-induced inversion of enantiomeric excess in organocatalytic selenylation of aldehydes. (2014) (28)
- Correction to Curtin–Hammett Paradigm for Stereocontrol in Organocatalysis by Diarylprolinol Ether Catalysts (2012) (28)
- What is the Order of a Reaction? (2017) (23)
- Kinetic Treatments for Catalyst Activation and Deactivation Processes based on Variable Time Normalization Analysis (2019) (23)
- Visual kinetic analysis † (2018) (22)
- Gold(III) complexes catalyze deoximations/transoximations at neutral pH. (2011) (18)
- Catalytic, PMe3-mediated conversion of secondary nitroalkanes to ketones: a very mild Nef-type process (2008) (15)
- Efficient preparation of N-phenylsulfenyl ketimines from oximes or nitro compounds without racemization of alpha-stereocenters. (2007) (14)
- Hydroarylation of alkenes by protonation/Friedel-Crafts trapping - HFIP-mediated access to per-aryl quaternary stereocentres. (2019) (12)
- Distribution of Catalytic Species as an Indicator To Overcome Reproducibility Problems. (2017) (12)
- Deciphering the roles of multiple additives in organocatalyzed Michael additions. (2016) (12)
- Reaction of Dess–Martin periodinane with 2-(alkylselenyl)pyridines. Dehydration of primary alcohols under extraordinarily mild conditions (2010) (12)
- Chirality-Induced Catalyst Aggregation: Insights into Catalyst Speciation and Activity Using Chiral Aluminum Catalysts in Cyclic Ester Ring-Opening Polymerization (2021) (11)
- AuBr3-catalyzed thiooxime-to-carbonyl conversion: from chiral aliphatic nitro compounds to ketones without racemization. (2009) (10)
- The interplay of thermodynamics and kinetics in dictating organocatalytic reactivity and selectivity (2013) (10)
- Gold(I)-catalyzed 1,3-O-transposition of ynones: Mechanism and catalytic acceleration with electron rich aldehydes (2018) (9)
- A bis(pyridyl)-N-alkylamine/Cu(i) catalyst system for aerobic alcohol oxidation. (2017) (9)
- Mechanistically Guided Design of an Efficient and Enantioselective Aminocatalytic α-Chlorination of Aldehydes (2021) (8)
- Use of Standard Addition to Quantify In Situ FTIR Reaction Data. (2020) (6)
- Catalytic Staudinger—Vilarrasa Reaction for the Direct Ligation of Carboxylic Acids and Azides. (2009) (5)
- Reaction monitoring reveals poisoning mechanism of Pd2(dba)3 and guides catalyst selection. (2017) (5)
- Dual H-bond activation of NHC-Au(I)-Cl complexes with amide functionalized side-arms assisted by H-bond donor substrates or acid additives. (2020) (3)
- Explaining Anomalies in Enamine Catalysis: “Downstream Species” as a New Paradigm for Stereocontrol (2016) (3)
- Kinetic Rationalization of Nonlinear Effects in Asymmetric Catalytic Cascade Reactions under Curtin–Hammett Conditions (2022) (2)
- Downstream Paradigm in Enamine Catalysis: Comment on “On Stereocontrol in Organocatalytic α-Chlorinations of Aldehydes” (2021) (1)
- Organic reaction mechanism classification using machine learning (2023) (1)
- Correction to "Intermediacy of Ni-Ni Species in sp2 C-O Bond Cleavage of Aryl Esters: Relevance in Catalytic C-Si Bond Formation". (2019) (1)
- Reaction of Dess—Martin Periodinane with 2‐(Alkylselenyl)pyridines. Dehydration of Primary Alcohols under Extraordinarily Mild Conditions. (2010) (1)
- Mechanistic interpretation of orders in catalyst greater than one (2022) (0)
- Organocatalytic Enantioselective α-Bromination of Aldehydes with N-Bromosuccinimide (2022) (0)
- A computational tool to accurately and quickly predict 19F NMR chemical shifts of molecules with fluorine-carbon and fluorine-boron bonds. (2022) (0)
- Efficient Preparation of N-Phenylsulfenyl Ketimines from Oximes or Nitro Compounds Without Racemization of α-Stereocenters. (2008) (0)
- The development of a Cu(I)/Bis(pyridyl)-N-alkylamine catalyst system for selective alcohol oxidation (2017) (0)
- Understanding the Diastereopreference of Intermediates in Aminocatalysis: Application to the Chiral Resolution of Lactols. (2021) (0)
- Electrospray ionization mass spectra of the reactions of NaAuBr₄ and related aurates with nucleophiles. (2014) (0)
- Catalytic, PMe3‐Mediated Conversion of Secondary Nitroalkanes to Ketones: A Very Mild Nef‐Type Process. (2008) (0)
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