162 results on '"Burés, Jordi"'
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2. Mechanistic interpretation of orders in catalyst greater than one
3. Aerobic Oxidative Coupling of 2‑Aminonaphthalenes by Homogenous Nonheme Iron Catalysts.
4. Bismuth‐Catalyzed Amide Reduction
5. Bismuth‐Catalyzed Amide Reduction
6. Mechanistic interpretation of orders in catalyst greater than one
7. What is the Order of a Reaction?
8. Organocatalytic Enantioselective α-Bromination of Aldehydes with N-Bromosuccinimide
9. Kinetic Rationalization of Nonlinear Effects in Asymmetric Catalytic Cascade Reactions under Curtin–Hammett Conditions
10. Preface
11. 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
12. Reversibility and reactivity in an acid catalyzed cyclocondensation to give furanochromanes – a reaction at the ‘oxonium-Prins’ vs. ‘ortho-quinone methide cycloaddition’ mechanistic nexus† †Electronic supplementary information (ESI) available: C. D.-T. Nielsen, W. J. Mooij, D. Sale, H. S. Rzepa, J. Burés and A. C. Spivey, FAIR data archives, Imperial College Research Computing Services data repository, 2018, DOI: 10.14469/hpc/3943 and sub-collections therein. See DOI: 10.1039/c8sc04302g
13. Mechanistically Guided Design of an Efficient and Enantioselective Aminocatalytic α-Chlorination of Aldehydes
14. Chirality-Induced Catalyst Aggregation: Insights into Catalyst Speciation and Activity Using Chiral Aluminum Catalysts in Cyclic Ester Ring-Opening Polymerization
15. Understanding the Diastereopreference of Intermediates in Aminocatalysis: Application to the Chiral Resolution of Lactols
16. Use of Standard Addition to Quantify In Situ FTIR Reaction Data
17. Dual H-bond activation of NHC–Au(i)–Cl complexes with amide functionalized side-arms assisted by H-bond donor substrates or acid additives
18. Correction to “Intermediacy of Ni–Ni Species in sp2 C–O Bond Cleavage of Aryl Esters: Relevance in Catalytic C–Si Bond Formation”
19. Kinetic Treatments for Catalyst Activation and Deactivation Processes based on Variable Time Normalization Analysis
20. Reversibility and reactivity in an acid catalyzed cyclocondensation to give furanochromanes – a reaction at the ‘oxonium-Prins’ vs. ‘ortho-quinone methide cycloaddition’ mechanistic nexus
21. Visual kinetic analysis
22. Use of Standard Addition to Quantify In Situ FTIR Reaction Data.
23. Intermediacy of Ni–Ni Species in sp2 C–O Bond Cleavage of Aryl Esters: Relevance in Catalytic C–Si Bond Formation
24. Gold(I)-Catalyzed 1,3-O-Transposition of Ynones: Mechanism and Catalytic Acceleration with Electron-Rich Aldehydes
25. The development of a Cu(I)/Bis(pyridyl)-N-alkylamine catalyst system for selective alcohol oxidation
26. Distribution of Catalytic Species as an Indicator To Overcome Reproducibility Problems
27. A bis(pyridyl)-N-alkylamine/Cu(i) catalyst system for aerobic alcohol oxidation
28. Reaction monitoring reveals poisoning mechanism of Pd2(dba)3 and guides catalyst selection
29. Variable Time Normalization Analysis: General Graphical Elucidation of Reaction Orders from Concentration Profiles
30. Ag(I)-Catalyzed C–H Activation: The Role of the Ag(I) Salt in Pd/Ag-Mediated C–H Arylation of Electron-Deficient Arenes
31. Explaining Anomalies in Enamine Catalysis: “Downstream Species” as a New Paradigm for Stereocontrol
32. A Simple Graphical Method to Determine the Order in Catalyst
33. Deciphering the roles of multiple additives in organocatalyzed Michael additions
34. Intermediacy of Ni–Ni Species in sp2 C–O Bond Cleavage of Aryl Esters: Relevance in Catalytic C–Si Bond Formation.
35. Reaction monitoring reveals poisoning mechanism of Pd2(dba)3 and guides catalyst selection.
36. Rationalization of an Unusual Solvent‐Induced Inversion of Enantiomeric Excess in Organocatalytic Selenylation of Aldehydes
37. Electrospray ionization mass spectra of the reactions of NaAuBr4and related aurates with nucleophiles
38. Intermediacy of Ni–Ni Species in sp2C–O Bond Cleavage of Aryl Esters: Relevance in Catalytic C–Si Bond Formation
39. The interplay of thermodynamics and kinetics in dictating organocatalytic reactivity and selectivity
40. Seebach’s oxazolidinone is a good catalyst for aldol reactions
41. Correction to Curtin–Hammett Paradigm for Stereocontrol in Organocatalysis by Diarylprolinol Ether Catalysts
42. Curtin–Hammett Paradigm for Stereocontrol in Organocatalysis by Diarylprolinol Ether Catalysts
43. Relative Tendency of Carbonyl Compounds To Form Enamines
44. Kinetic correlation between aldehyde/enamine stereoisomers in reactions between aldehydes with α-stereocenters and chiral pyrrolidine-based catalysts
45. Enamine Carboxylates as Stereodetermining Intermediates in Prolinate Catalysis
46. Mechanistic Rationalization of Organocatalyzed Conjugate Addition of Linear Aldehydes to Nitro-olefins
47. Gold(III) Complexes Catalyze Deoximations/Transoximations at Neutral pH
48. Reaction of Dess–Martin periodinane with 2-(alkylselenyl)pyridines. Dehydration of primary alcohols under extraordinarily mild conditions
49. AuBr3-Catalyzed Thiooxime-to-Carbonyl Conversion: From Chiral Aliphatic Nitro Compounds to Ketones without Racemization
50. Catalytic Staudinger—Vilarrasa Reaction for the Direct Ligation of Carboxylic Acids and Azides
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