Electrocarboxylation of benzyl chlorides at silver cathode at the preparative scale level

[1]  M. Sabatino,et al.  Electrocarboxylation of aromatic ketones: Influence of operative parameters on the competition between ketyl and ring carboxylation , 2007 .

[2]  P. Mussini,et al.  Relevance of electron transfer mechanism in electrocatalysis: the reduction of organic halides at silver electrodes. , 2006, Chemical communications.

[3]  C. Amatore,et al.  Electrocarboxylation of benzyl halides through redox catalysis on the preparative scale. , 2006, Chemistry.

[4]  C. Amatore,et al.  CO2 as a C1-organic building block : Electrocarboxylation of aromatic ketones. A quantitative study of the effect of the concentration of substrate and of carbon dioxide on the selectivity of the process , 2006 .

[5]  P. Mussini,et al.  Electrochemical reduction of benzyl halides at a silver electrode , 2006 .

[6]  P. Poizot,et al.  A copper–palladium alloy usable as cathode material mode of formation and first examples of catalytic cleavages of carbon–halide bonds , 2006 .

[7]  A. Gennaro,et al.  Electrocatalytic reduction of arylethyl chlorides at silver cathodes in the presence of carbon dioxide: Synthesis of 2-arylpropanoic acids , 2005 .

[8]  P. Mussini,et al.  Building up an electrocatalytic activity scale of cathode materials for organic halide reductions , 2005 .

[9]  O. Scialdone,et al.  INFLUENCE OF THE EXPERIMENTAL SYSTEM AND OPTIMIZATION OF THE SELECTIVITY FOR THE ELECTROCARBOXYLATION OF CHLOROACETONITRILE TO CYANOACETIC ACID , 2004 .

[10]  A. Gennaro,et al.  Electrocatalytic synthesis of 6-aminonicotinic acid at silver cathodes under mild conditions , 2004 .

[11]  J. Savéant,et al.  Successive Removal of Chloride Ions from Organic Polychloride Pollutants. Mechanisms of Reductive Electrochemical Elimination in Aliphatic Gem-Polychlorides, α,β-Polychloroalkenes, and α,β-Polychloroalkanes in Mildly Protic Medium , 2003 .

[12]  S. Verevkin,et al.  Thermodynamic properties of benzyl halides: enthalpies of formation, strain enthalpies, and carbon–halogen bond dissociation enthalpies , 2003 .

[13]  A. Gennaro,et al.  Homogeneous electron transfer catalysis in the electrochemical carboxylation of arylethyl chlorides , 2003 .

[14]  A. Gennaro,et al.  Dissociative electron transfer to haloacetonitriles. An example of the dependency of in-cage ion-radical interactions upon the leaving group. , 2002, Journal of the American Chemical Society.

[15]  A. Gennaro,et al.  Estimation of the standard reduction potentials of some 1-arylethyl radicals in acetonitrile , 2002 .

[16]  M. Fedurco,et al.  Ab Initio and Electrochemical Studies on the Reductive Bond Dissociation in Haloethanols , 2002 .

[17]  J. Damodar,et al.  Synthesis of 2-arylpropionic acids by electrocarboxylation of benzylchlorides catalysed by PdCl2(PPh3)2 , 2001 .

[18]  P. Mussini,et al.  Silver as a powerful electrocatalyst for organic halide reduction: the critical role of molecular structure , 2001 .

[19]  A. Gennaro,et al.  Nickel(I)(salen)-electrocatalyzed reduction of benzyl chlorides in the presence of carbon dioxide , 2001 .

[20]  J. Savéant,et al.  Stepwise and concerted pathways in photoinduced and thermal electron-transfer/bond-breaking reactions. experimental illustration of similarities and contrasts. , 2001, Journal of the American Chemical Society.

[21]  M. Fedurco,et al.  Reductive Cleavage of the Carbon−Halogen Bond in Simple Methyl and Methylene Halides. Reactions of the Methyl Radical and Carbene at the Polarized Electrode/Aqueous Solution Interface , 2001 .

[22]  P. Mussini,et al.  Electrocatalytic potentialities of silver as a cathode for organic halide reductions , 2000 .

[23]  G. Gritzner.  Single-ion transfer properties: a measure of ion-solvation in solvents and solvent mixtures , 1998 .

[24]  Ch. Lambrou,et al.  Electrochemical reduction of dichloromethane to higher hydrocarbons , 1998 .

[25]  S. Antonello,et al.  Electroreduction of Dialkyl Peroxides. Activation-Driving Force Relationships and Bond Dissociation Free Energies. , 1997 .

[26]  J. Savéant.  Dynamics of Cleavage and Formation of Anion Radicals into and from Radicals and Nucleophiles. Structure-Reactivity Relationships in SRN1 Reactions , 1994 .

[27]  C. Amatore,et al.  Carbon dioxide as a C1 building block. Mechanism of palladium-catalyzed carboxylation of aromatic halides , 1992 .

[28]  J. Savéant,et al.  Electron Transfer and Bond Breaking. Examples of Passage from a Sequential to a Concerted Mechanism in the Electrochemical Reductive Cleavage of Arylmethyl Halides , 1992 .

[29]  S. Gambino,et al.  Use of Sacrificial Anodes in Synthetic Electrochemistry. Processes Involving Carbon Dioxide , 1992 .

[30]  A. Gennaro,et al.  Solubility and electrochemical determination of CO2 in some dipolar aprotic solvents , 1990 .

[31]  D. Griller,et al.  Thermodynamic significance of .rho.+ and .rho.- from substituent effects on the redox potentials of arylmethyl radicals , 1990 .

[32]  Christian Amatore,et al.  Nickel-catalysed electrosynthesis of anti-inflammatory agents. III. A new electrolyser for organic solvents; oxidation of metal powder as an alternative to sacrificial anodes , 1990 .

[33]  J. Périchon,et al.  Electrosynthesis of carboxylic acids from organic halides and carbon dioxide , 1985 .

[34]  S. Gambino,et al.  Sacrificial Anodes in the Electrocarboxylation of Organic Chlorides , 1984 .

[35]  F. Murrieta-Guevara,et al.  Solubility of carbon dioxide, hydrogen sulfide, and methane in pure and mixed solvents , 1984 .

[36]  M. Baird,et al.  Cyclopropene-carbene rearrangements at low temperatures. Generation and trapping of 1,2-dichloro-3-methylbut-2-en-1-ylidene , 1984 .

[37]  J. Savéant,et al.  Mechanism and kinetic characteristics of the electrochemical reduction of carbon dioxide in media of low proton availability , 1981 .

[38]  J. Savéant,et al.  Product distribution in preparative scale electrolysis: Part I. Introduction , 1981 .

[39]  Jean-Michel Savéant,et al.  Standard potential and kinetic parameters of the electrochemical reduction of carbon dioxide in dimethylformamide , 1977 .

[40]  John L. Chruma,et al.  Electrolytic reductive coupling. XXI. Reduction of organic halides in the presence of electrophiles , 1972 .

[41]  R. Bridger,et al.  Directive Effects in the Attack of Phenyl Radicals on Carbon-Hydrogen Bonds , 1963 .

[42]  J. Simonet.  The one-electron reduction of primary alkyl iodides at palladium and palladiated surfaces: a facile source of alkyl radicals? , 2005 .

[43]  A. Gennaro,et al.  Electrocatalytic carboxylation of benzyl chlorides at silver cathodes in acetonitrile. , 2002, Chemical communications.

[44]  Zeev B. Alfassi,et al.  General aspects of the chemistry of radicals , 1999 .

[45]  T. Shono,et al.  PERFORMANCES OF HOMOGENEOUS CHARGE TRANSFER CATALYSTS IN THE ELECTROCARBOXYLATION OF BENZYL HALIDES , 1999 .

[46]  C. Tommos,et al.  ON RADICAL ANIONS IN ELUCIDATION OF MECHANISMS OF ORGANIC REACTIONS , 1997 .

[47]  D. Iarossi,et al.  Reductive electron transfer on trichloromethyl derivatives of benzene and pyridine studied by electrochemical methods , 1997 .

[48]  A. Gennaro,et al.  Electrochemical carboxylation of arylmethyl chlorides catalysed by [Co(salen)][H2salen =N,N′-bis(salicylidene)ethane-1,2-diamine] , 1996 .

[49]  Jean-Michel Savéant,et al.  Mechanism of the electrochemical reduction of carbon dioxide at inert electrodes in media of low proton availability , 1996 .

[50]  M. Aresta,et al.  Enzymatic and model carboxylation and reduction reactions for carbon dioxide utilization : proceedings of the NATO Advanced Study Institute on Enzymatic and Model Carboxylation and Reduction Reactions for Carbon Dioxide Utilization, Riva dei Tessali, Italy, June 17-28, 1989 , 1990 .

[51]  A. Jutand,et al.  Nickel catalysed electrosynthesis of anti-inflammatory agents. Part II — Monitoring of the electrolyses by HPLC analysis. Role of the catalyst , 1988 .

[52]  J. Fauvarque,et al.  Nickel catalysed electrosynthesis of anti-inflammatory agents. Part I — Synthesis of aryl-2 propionic acids, under galvanostatic conditions , 1988 .

[53]  M. Aresta,et al.  Carbon Dioxide as a Source of Carbon : Biochemical and Chemical Uses , 1987 .

[54]  J. A. Franz,et al.  Absolute rate constants for hydrogen atom abstraction by benzyl radical from thiophenol, tributylstannane, tributylstannane-d, and dicyclohexylphosphine and for the cyclization of the 2-allylbenzyl radical , 1986 .