All Stories

  1. The Role of Catalyst Formation–Deactivation Processes and Evidence for a Nonlinear Mechanism in the Mizoroki–Heck Reaction with Aryl Chlorides
  2. Fast reversible oxidative addition of demanding aryl chlorides to Pd under real conditions of catalysis in the Mizoroki-Heck reaction: The kinetic proof
  3. The adequacy of the observed kinetic order in catalyst and the differential selectivity patterns to the hypothesis of the cooperative mechanism of catalysis of the Suzuki—Miyaura reaction
  4. Experimental evidence for the direct involvement of Pd(0) and Pd(II) anionic phosphine complexes in the Mizoroki–Heck coupling reaction
  5. Activation of Aryl Chlorides in the Suzuki-Miyaura Reaction by “Ligand-Free” Pd Species through a Homogeneous Catalytic Mechanism: Distinguishing between Homogeneous and Heterogeneous Catalytic Mechanisms
  6. Discrimination of the mechanistic hypotheses for two- and three-component cross-coupling reactions by using mathematical modeling of the differential selectivity patterns
  7. A Study of the Step of Alkene Activation under Ligand-Free Conditions in the Mizoroki–Heck Reaction with Unreactive Aryl Chlorides
  8. Ligand-Free Catalytic Cross-Coupling in the System Aryl Halide–Arylacetylene–Alkene
  9. Nonclassical cooperative mechanism in Suzuki-Miyaura reaction – Is it possible?
  10. Is oxidative addition indeed the rate-determining step of the Suzuki–Miyaura reaction with less-reactive aryl chlorides under “ligand-free” conditions?
  11. Is the Mechanistic Scheme of the Heck‐Type Coupling with Unsaturated Substrates needed to be revised?
  12. Analysis of Differential Selectivity Using Phase Trajectories of Catalytic Reactions: New Aspects and Applications
  13. A Kinetic Study of the Step of Aryl Halide Activation in a Direct Arylation Reaction of Indole under Real Catalysis Conditions
  14. Polyaromatic Products of Three-Component Coupling of Aryl Halide with Two Molecules of Arylacetylene and Arylboronic Acid under Ligand-Free Catalysis Conditions
  15. Distinguishing between Homogeneous and Heterogeneous Catalytic Activity in C–H Arylation of an Indole with Aryl Halides under “Ligandless” Conditions: Crucial Evidence from Real Catalytic Experiments
  16. The role of phosphine ligands in the catalytic systems of the Heck reaction with aromatic carboxylic anhydrides
  17. Mechanistic Study of Catalysis in the Mizoroki–Heck Reaction with Anhydrides of Aromatic Acids
  18. Mechanistic Study of Direct Arylation of Indole Using Differential Selectivity Measurements: Shedding Light on the Active Species and Revealing the Key Role of Electrophilic Substitution in the Catalytic Cycle
  19. Composition and Properties of Brown Coal from the Bodonskoe Deposit in Buryatia
  20. Direct Kinetic Evidence for the Active Anionic Palladium(0) and Palladium(II) Intermediates in the Ligand-Free Heck Reaction with Aromatic Carboxylic Anhydrides
  21. Kinetic aspects of operando studies: state-of-the-art and unexplored possibilities
  22. Kinetic investigation of cross-coupling reaction steps by advanced competing reaction methods
  23. Formation of polyaromatic compounds by coupling of aryl iodides with arylacetylenes in the presence of palladium-based ligand-free catalytic systems
  24. Trace elements in the coals of Eastern Siberia
  25. Role of the base and endogenous anions in “ligand-free” catalytic systems for the Suzuki–Miyaura reaction
  26. Measuring the kinetic isotope effect at natural isotopic abundances for discriminating between the homogeneous and heterogeneous catalytic mechanisms in the Heck and Suzuki reactions
  27. Study of the differential selectivity of cross-coupling reactions for elucidating the nature of the true catalyst
  28. Direct arylation and heterogeneous catalysis; ever the twain shall meet
  29. Differential selectivity measurements and competitive reaction methods as effective means for mechanistic studies of complex catalytic reactions
  30. Adsorption properties of coal from the Ishideiskoe deposit, semicokes, and ash and slag wastes from the combustion of coals from Siberia and Sakhalin
  31. Approach to the Determination of Kinetic Order of Catalyst Deactivation: Observation of Unusual Kinetics in the Suzuki – Miyaura Reaction
  32. Mechanistic studies of the Suzuki-Miyaura reaction with aryl bromides using Pd supported on micro- and mesoporous activated carbons
  33. Distinguishing between the homogeneous and heterogeneous mechanisms of catalysis in the Mizoroki-Heck and Suzuki-Miyaura reactions: Problems and prospects
  34. competing reaction method for identification of fast and slow steps of catalytic cycles: Application to heck and Suzuki reactions
  35. Simple kinetic method for distinguishing between homogeneous and heterogeneous mechanisms of catalysis, illustrated by the example of “ligand-free” Suzuki and Heck reactions of aryl iodides and aryl bromides
  36. Coals from the Khingui coal manifestation
  37. Role of a base in Suzuki-Miyaura reaction
  38. In situ NMR studies of the mechanism of homogeneously and heterogeneously catalysed Heck reactions of aryl chlorides and bromides
  39. Characterization of coals from the Luzhki section of the Zabitui deposit
  40. Suzuki reaction with aryl bromides at room temperature in the presence of a simple “ligand-free” catalytic system
  41. Study of “ligand-free” catalytic systems with low palladium content for the Heck reaction
  42. Polymerization of acetylene in aqueous PdCl2-CuCl solutions: Novel catalytically active palladium-copper-containing carbon materials
  43. Problems of distinguishing the homogeneous and heterogeneous mechanisms of the Suzuki reaction
  44. Suzuki reaction: mechanistic multiplicity versus exclusive homogeneous or exclusive heterogeneous catalysis
  45. State of palladium in ligandless catalytic systems for the Heck reaction of nonactivated bromobenzene
  46. New approaches to heck reaction testing for homogeneity-heterogeneity
  47. Enhancement of catalyst performance in Heck reaction of nonactivated aryl bromides in the absence of phosphine ligands
  48. Heck reactions of alkenes with aryl iodides and aryl bromides: Rate-determining steps deduced from a comparative kinetic study of competing and noncompeting reactions
  49. Kinetics of the Heck reactions of styrene with bromobenzene and iodobenzene in the presence of ligandless catalytic systems: A comparative study
  50. Interplays between Reactions within and without the Catalytic Cycle of the Heck Reaction as a Clue to the Optimization of the Synthetic Protocol
  51. 2-Arylazo-1-vinylpyrroles: A Novel Promising Family of Reactive Dyes
  52. Effect of macrokinetic factors on the ligand-free Heck reaction with non-activated bromoarenes
  53. Oxidative Addition Step in Reactions Involving Palladium Activation of Carbon-Halogen and Carbon-Oxygen Bonds
  54. Concept of ?magic? number clusters as a new approach to the interpretation of unusual kinetics of the Heck reaction with aryl bromides
  55. Role of catalyst deactivation and regeneration in the heck reaction involving unactivated aryl bromides
  56. Role of catalyst deactivation and regeneration in the heck reaction involving unactivated aryl bromides
  57. Simple method for enhancement of the ligand-free palladium catalyst activity in the Heck reaction with non-activated bromoarenes
  58. Reducing agents as components in catalytic systems of the Heck reaction
  59. Regioselective ?-arylation ofN-vinylpyrroles by the Heck reaction
  60. Effect of base on the state of palladium in the synthesis of styrene in the heck reaction