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http://hub.abes.fr/acs/periodical/joceah/1991/volume_56/issue_16/101021jo00016a008/authorship/6
http://hub.abes.fr/acs/periodical/joceah/1991/volume_56/issue_2/101021jo00002a020/authorship/3
http://hub.abes.fr/acs/periodical/jpchax/1995/volume_99/issue_38/101021j100038a029/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1992/volume_114/issue_14/101021ja00040a074/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/1993/volume_115/issue_17/101021ja00070a026/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/1995/volume_117/issue_46/101021ja00151a012/authorship/5
http://hub.abes.fr/acs/periodical/jacsat/1985/volume_107/issue_12/101021ja00298a009/authorship/3
http://hub.abes.fr/acs/periodical/cmatex/2005/volume_17/issue_15/101021cm050339q/authorship/4
http://hub.abes.fr/acs/periodical/jpcbfk/2006/volume_110/issue_39/101021jp063368c/authorship/2
http://hub.abes.fr/acs/periodical/langd5/2001/volume_17/issue_22/101021la010486c/authorship/2
http://hub.abes.fr/acs/periodical/langd5/2003/volume_19/issue_15/101021la030046g/authorship/3
http://hub.abes.fr/acs/periodical/cmatex/2006/volume_18/issue_8/101021cm052065c/authorship/4
http://hub.abes.fr/acs/periodical/langd5/2005/volume_21/issue_10/101021la046912m/authorship/9
http://hub.abes.fr/acs/periodical/cmatex/2002/volume_14/issue_1/101021cm011212d/authorship/4
http://hub.abes.fr/acs/periodical/cmatex/2003/volume_15/issue_18/101021cm034167d/authorship/5
http://hub.abes.fr/acs/periodical/langd5/2004/volume_20/issue_19/101021la049194c/authorship/4
http://hub.abes.fr/acs/periodical/cmatex/2002/volume_14/issue_11/101021cm0211397/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/2008/volume_130/issue_27/101021ja8018912/authorship/3
http://hub.abes.fr/acs/periodical/jpccck/2008/volume_112/issue_47/101021jp807044j/authorship/4
http://hub.abes.fr/acs/periodical/cmatex/2005/volume_17/issue_3/101021cm0490625/authorship/6
http://hub.abes.fr/acs/periodical/cmatex/2007/volume_19/issue_18/101021cm0700551/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/2001/volume_123/issue_19/101021ja003276f/authorship/7
http://hub.abes.fr/acs/periodical/langd5/2005/volume_21/issue_1/101021la048106l/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/1981/volume_103/issue_23/101021ja00413a028/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1993/volume_58/issue_10/101021jo00062a007/authorship/5
http://hub.abes.fr/acs/periodical/jacsat/1980/volume_102/issue_12/101021ja00532a023/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1990/volume_112/issue_9/101021ja00165a040/authorship/4
http://hub.abes.fr/acs/periodical/joceah/1986/volume_51/issue_20/101021jo00370a003/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/1982/volume_104/issue_7/101021ja00371a030/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/1985/volume_107/issue_17/101021ja00303a007/authorship/3
http://hub.abes.fr/acs/periodical/joceah/1983/volume_48/issue_17/101021jo00165a013/authorship/4
http://hub.abes.fr/acs/periodical/joceah/1988/volume_53/issue_7/101021jo00242a029/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/1994/volume_116/issue_11/101021ja00090a013/authorship/5
http://hub.abes.fr/acs/periodical/jacsat/1984/volume_106/issue_21/101021ja00333a034/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/1991/volume_113/issue_18/101021ja00018a025/authorship/2
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Electrochemically induced nucleophilic substitution of perfluoroalkyl halides. An example of a dissociative electron-transfer-induced chemical reaction
Electrochemically catalyzed aromatic nucleophilic substitution. Phenoxide ion as nucleophile
Nucleophile and aryl radical reactivity in SRN1 aromatic nucleophilic substitution reactions. Absolute and relative electrochemical determination
Covalent modification of carbon surfaces by grafting of functionalized aryl radicals produced from electrochemical reduction of diazonium salts
Nonchain Processes in Nucleophilic Substitutions Triggered by Electron Transfer (SRN1). Photochemical and Electrochemical Induction of the Substitution of 1-Iodoadamantane by Arenethiolate Ions
Electron-transfer-induced reactions. A novel approach based on electrochemical redox catalysis. Application to aromatic nucleophilic substitutions
Dissociative Electron Transfer to Dihaloalkanes. Electrochemical Reduction of 1,3-Dihaloadamantanes, 1,4-Dihalobicyclo[2.2.2]octanes, and 1,3-Dihalobicyclo[1.1.1]pentanes
Hydrogen atom transfer oxidation of primary and secondary alcoholates into aldehydes and ketones by aromatic halides in liquid ammonia. A new electrochemically induceable reaction
Sterically Hindered Diazonium Salts for the Grafting of a Monolayer on Metals
Electrochemical Attachment of Organic Groups to CarbonFelt Surfaces
Covalent Modification of Iron Surfaces by Electrochemical Reductionof Aryldiazonium Salts
Formation of Polyphenylene Films on Metal Electrodes byElectrochemical Reduction of Benzenediazonium Salts
The Electrochemical Reduction of Diazonium Salts onIron Electrodes. The Formation of Covalently BondedOrganic Layers and Their Effect on Corrosion
X-ray Photoelectron Spectroscopy Evidence forthe Covalent Bond between an Iron Surfaceand Aryl Groups Attached by theElectrochemical Reduction of Diazonium Salts
Electrochemical Oxidation of Aliphatic Amines and TheirAttachment to Carbon and Metal Surfaces
Attachment of Polymers to Organic Moieties CovalentlyBonded to Iron Surfaces
Spontaneous Grafting of Iron Surfaces by Reduction ofAryldiazonium Salts in Acidic or Neutral Aqueous Solution.Application to the Protection of Iron against Corrosion
Time-of-Flight Secondary Ion Mass SpectroscopyCharacterization of the Covalent Bonding between aCarbon Surface and Aryl Groups
Novel Approach for Metallic Surface-Initiated AtomTransfer Radical Polymerization Using ElectrograftedInitiators Based on Aryl Diazonium Salts
Grafting of Nitrophenyl Groups on Carbon and Metallic Surfaceswithout Electrochemical Induction
Spontaneous Attachment of Amines to Carbon and Metallic Surfaces
Organic Layers Bonded to Industrial, Coinage, andNoble Metals through Electrochemical Reduction ofAryldiazonium Salts
Electro- and Photografting of Carbon or Metal Surfaces by Alkyl Groups
Surface Modification of Conducting Substrates. Existence of AzoBonds in the Structure of Organic Layers Obtained from DiazoniumSalts
Outer-sphere dissociative electron transfer to organic molecules: a source of radicals or carbanions? Direct and indirect electrochemistry of perfluoroalkyl bromides and iodides
The solvent as hydrogen-atom donor in organic electrochemical reactions. Reduction of aromatic halides
Determination of formal potentials of chemically unstable redox couples by second-harmonic alternating current voltammetry and cyclic voltammetry. Application to the oxidation of thiophenoxide ions
Electrochemical reductive carboxylation: reduction of unsaturated compounds in the presence of methyl chloroformate
Very fast, in-cage, recombination of a radical with a nucleophile. Arylazo sulfides in SRN1 aromatic nucleophilic substitutions
Electron-transfer-induced reactions. Termination steps and efficiency of the chain process in SRN1 aromatic substitutions
Electrochemically induced SRN1 aromatic nucleophilic substitution. Absolute reactivities of phenyl derivatives in liquid ammonia
Hydroxylation by Electrochemically Generated OH.bul. Radicals. Mono- and Polyhydroxylation of Benzoic Acid: Products and Isomer Distribution
Electrochemically induced aromatic substitution. The 2-nitropropane anion, a powerful nucleophile in SRN1 aromatic substitution
Aryl radicals from electrochemical reduction of aryl halides. Addition on olefins
Electrochemical and chemical reduction of furopyrazines, thienopyrazines, furoquinoxalines and thienoquinoxalines
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