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http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_1/101021jo702091e/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1995/volume_60/issue_19/101021jo00124a006/authorship/2
http://hub.abes.fr/acs/periodical/bichaw/2005/volume_44/issue_49/101021bi051127/authorship/6
http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_21/101021jo035001z/authorship/2
http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_5/101021jo005707i/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/2001/volume_123/issue_38/101021ja016092p/authorship/1
http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_8/101021jo010102n/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/2006/volume_128/issue_46/101021ja066692u/authorship/6
http://hub.abes.fr/acs/periodical/jacsat/2002/volume_124/issue_20/101021ja016874i/authorship/3
http://hub.abes.fr/acs/periodical/joceah/2006/volume_71/issue_13/101021jo060780f/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_36/101021ja053654m/authorship/5
http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_16/101021jo800938d/authorship/2
http://hub.abes.fr/acs/periodical/langd5/2003/volume_19/issue_16/101021la034188m/authorship/3
http://hub.abes.fr/acs/periodical/joceah/1993/volume_58/issue_11/101021jo00063a064/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1993/volume_58/issue_5/101021jo00057a005/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1991/volume_56/issue_17/101021jo00017a049/authorship/3
http://hub.abes.fr/acs/periodical/joceah/1992/volume_57/issue_12/101021jo00038a013/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1993/volume_58/issue_4/101021jo00056a026/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1994/volume_116/issue_21/101021ja00100a073/authorship/2
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Mechanism of nucleophilic substitution reactions of o-nitrobenzenesulfenamides: evidence for a substitution proceeding through a sulfuranide intermediate
The markedly enhanced basicity of selenenamides vs sulfenamides and the mechanism of the methanolysis of o-nitro- and 2,4,6-tri-tert-butylbenzeneselenenamides
Excited State Reactivity as a Function of Diradical Structure. Evidence for Two Triplet Cyclopropyldicarbinyl Diradical Intermediates with Differing Reactivity
A simple new synthesis of thiobisamines
Photoinduced Signal Amplification through Controlled Externally SensitizedFragmentation in Masked Sensitizers
Effect of β-Alkylthioethyl Substitution in 1,3-Dithianes: Quasianchimeric Assistance in Photoinduced Electron Transfer?
Conformational Analysis of Singlet−Triplet State Mixing inPaternò−Büchi Diradicals
2,6,7-Trithiabicyclo[2.2.2]octanes as PromisingPhotolabile Tags for Combinatorial Encoding
When Ethyl Is Infinitely Different from Methyl: Double Addition of Lithiated Dithianes toAromatic Carboxylates Revisited
Investigation of the Binding Geometry of a Peripheral Membrane Protein
Dithiane-Based Photolabile Amphiphiles: TowardPhotolabile Liposomes1,2
Release and Report: A New Photolabile Caging System with a Two-PhotonFluorescence Reporting Function
Photoinduced C−C Bond Cleavage inDithiane−Carbonyl Adducts: A Laser FlashPhotolysis Study
Liposomes from Novel Photolabile Phospholipids: Light-Induced Unloadingof Small Molecules As Monitored by PFG NMR
Photoinduced 1,3-Proton Shift inMethyldithiepines as a Potential Way ofModulating Hyperpolarizabilities
Anomalous C−C Bond Cleavage inSulfur-Centered Cation RadicalsContaining a Vicinal Hydroxy Group
A one-pot trifunctionalization of olefins with benzeneseleninic and trifluoroacetic anhydrides using a commonly undesirable side reaction as a key step. [Erratum to document cited in CA118(19):191881a]
A one-pot trifunctionalization of olefins with benzeneseleninic and trifluoroacetic anhydrides using a commonly undesirable side reaction as a key step
Novel Dissection Analysis of Spin-Orbit Coupling in the Type-B Cyclohexenone Photorearrangement. What Controls Photoreactivity? Mechanistic and Exploratory Organic Photochemistry
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