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http://hub.abes.fr/acs/periodical/joceah/2006/volume_71/issue_5/101021jo052463z/authorship/2
http://hub.abes.fr/acs/periodical/chreay/2007/volume_107/issue_6/101021cr068352x/authorship/1
http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_19/101021jo010469s/authorship/4
http://hub.abes.fr/acs/periodical/joceah/2004/volume_69/issue_3/101021jo035679e/authorship/2
http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_4/101021jo7019509/authorship/2
http://hub.abes.fr/acs/periodical/joceah/2000/volume_65/issue_2/101021jo990817e/authorship/3
http://hub.abes.fr/acs/periodical/ancham/2006/volume_78/issue_12/101021ac060455s/authorship/2
http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_12/101021jo034375p/authorship/2
http://hub.abes.fr/acs/periodical/joceah/2005/volume_70/issue_2/101021jo048413w/authorship/2
http://hub.abes.fr/acs/periodical/achre4/2005/volume_38/issue_9/101021ar0402356/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/2006/volume_128/issue_33/101021ja0627287/authorship/2
http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_22/101021jo010400k/authorship/2
http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_3/101021jo026516d/authorship/3
http://hub.abes.fr/acs/periodical/joceah/2004/volume_69/issue_10/101021jo049770/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/2003/volume_125/issue_43/101021ja036000r/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/2007/volume_129/issue_17/101021ja068647s/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/2007/volume_129/issue_37/101021ja075050j/authorship/4
http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_19/101021jo0104680/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/2007/volume_129/issue_51/101021ja074778x/authorship/5
http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_1/101021jo7020218/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/1995/volume_117/issue_30/101021ja00135a004/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1994/volume_59/issue_19/101021jo00098a019/authorship/2
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Photocatalysis for the Formation of the C−C Bond
Photochemical Alkylation of Ketene Dithioacetal S,S-Dioxides. AnExample of Captodative Olefin Functionalization
Phenonium Ions from the Addition of Phenyl Cations to Alkenes.Photochemical Synthesis of (Rearranged) Aminoalkylanilinesfrom Haloanilines in the Presence of Alkenes and Amines
Using Phenyl Cations as Probes for EstablishingElectrophilicity−Nucleophilicity Relations
Homolytic vs Heterolytic Paths in the Photochemistry ofHaloanilines
A Meta Effect in Organic Photochemistry? The Case of SN1Reactions in Methoxyphenyl Derivatives
A Meta Effect in Organic Photochemistry? The Caseof SN1 Reactions in Methoxyphenyl Derivatives [J. Am. Chem. Soc.2007, 129, 5605−5611].
Hydrocarbon Activation. Synthesis of β-Cycloalkyl (Di)nitrilesthrough Photosensitized Conjugate Radical Addition
A Novel α-Arylation of Ketones, Aldehydes, and Esters via aPhotoinduced SN1 Reaction through 4-Aminophenyl Cations
Arylation Reactions: ThePhoto-SN1 Path via PhenylCation as an Alternative toMetal Catalysis
Multiwalled Carbon Nanotube Chemically ModifiedGold Electrode for Inorganic As Speciation andBi(III) Determination
Generation and Reactivity of the 4-Aminophenyl Cation byPhotolysis of 4-Chloroaniline
(Sensitized) Photolysis of Diazonium Salts as a Mild GeneralMethod for the Generation of Aryl Cations. Chemoselectivity ofthe Singlet and Triplet 4-Substituted Phenyl Cations
Intramolecular Electron Transfer in the Photochemistry of SomeNitrophenyldihydropyridines
Benzyl (Phenyl) γ- and δ-lactones via Photoinduced Tandem Ar−C, C−OBond Formation
The β Effect of Silicon in Phenyl Cations
Aryl Cations from Aromatic Halides. Photogeneration andReactivity of 4-Hydroxy(methoxy)phenyl Cation
Photoinduced, Ionic Meerwein Arylation of Olefins
Hammett Correlations in the Photosensitized Oxidation of4-Substituted Thioanisoles
Geometry and Energy of Substituted Phenyl Cations
Radicals through Photoinduced Electron Transfer. Addition to Olefin and Addition to Olefin-Aromatic Substitution Reactions
Radical Addition to Alkenes via Electron Transfer Photosensitization
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