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http://hub.abes.fr/acs/periodical/jpchax/1992/volume_96/issue_11/101021j100190a102/authorship/1
http://hub.abes.fr/acs/periodical/jpchax/1992/volume_96/issue_23/101021j100202a023/authorship/1
http://hub.abes.fr/acs/periodical/jpcafh/2007/volume_111/issue_1/101021jp064066d/authorship/5
http://hub.abes.fr/acs/periodical/jpcafh/2003/volume_107/issue_4/101021jp026521l/authorship/3
http://hub.abes.fr/acs/periodical/chreay/2006/volume_106/issue_12/101021cr050964e/authorship/2
http://hub.abes.fr/acs/periodical/orgnd7/1996/volume_15/issue_24/101021om960343z/authorship/3
http://hub.abes.fr/acs/periodical/orgnd7/2008/volume_27/issue_20/101021om800578c/authorship/4
http://hub.abes.fr/acs/periodical/jpcafh/2008/volume_112/issue_50/101021jp802839n/authorship/6
http://hub.abes.fr/acs/periodical/joceah/2006/volume_71/issue_17/101021jo052551j/authorship/3
http://hub.abes.fr/acs/periodical/orgnd7/2003/volume_22/issue_23/101021om030343g/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/2008/volume_130/issue_26/101021ja801159v/authorship/5
http://hub.abes.fr/acs/periodical/orgnd7/2001/volume_20/issue_5/101021om000885n/authorship/4
http://hub.abes.fr/acs/periodical/orgnd7/1996/volume_15/issue_7/101021om9508804/authorship/2
http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_6/101021jo0701886/authorship/3
http://hub.abes.fr/acs/periodical/cmatex/2002/volume_14/issue_8/101021cm0112993/authorship/5
http://hub.abes.fr/acs/periodical/orgnd7/2002/volume_21/issue_5/101021om010568w/authorship/7
http://hub.abes.fr/acs/periodical/joceah/2006/volume_71/issue_19/101021jo061097w/authorship/3
http://hub.abes.fr/springer/periodical/10910/1994/volume_16/issue_1/B8DE1935FC3A343AE053120B220A75A4/authorship/1
http://hub.abes.fr/springer/periodical/10910/1995/volume_17/issue_2/B8DE1935FB79343AE053120B220A75A4/authorship/1
http://hub.abes.fr/springer/periodical/10910/1996/volume_19/issue_2/B8DE1935FCF6343AE053120B220A75A4/authorship/1
http://hub.abes.fr/springer/periodical/10910/1994/volume_16/issue_1/B8DE1935FC2B343AE053120B220A75A4/authorship/1
http://hub.abes.fr/springer/periodical/10910/1995/volume_17/issue_2/B8DE1935FB73343AE053120B220A75A4/authorship/1
http://hub.abes.fr/springer/periodical/10910/1994/volume_16/issue_1/B8DE1935FC28343AE053120B220A75A4/authorship/1
http://hub.abes.fr/springer/periodical/10910/1994/volume_16/issue_1/B8DE1935FC37343AE053120B220A75A4/authorship/1
http://hub.abes.fr/springer/periodical/10910/1995/volume_17/issue_2/B8DE1935FB7A343AE053120B220A75A4/authorship/1
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Explicit periodic trend of van der Waals radii
Chemical algebra. I: Fuzzy subgroups
Chemical algebra. VI:G-weighted metrics of non-compact groups: Group of translations in the Euclidean space
α-Iminoacyl Ligands in Carbonylmetalates
Description of Carbo-oxocarbons and Assessment of Exchange-Correlation Functionals forthe DFT Description of Carbo-mers
From Macrocyclic Oligo-acetylenes to Aromatic Ring Carbo-mers
Parallel Approaches to Mono- and Bis-PropargylicActivation via Co2(CO)8 and [Ru3(μ-Cl)(CO)10]-
Direct Evaluation of Cyclic Contributions to the π Energy of Conjugated Hydrocarbons from Strongly Localized Zero-Order Pictures
Trimesitylmethylphosphonium Cation. Supramolecular Stereocontrol and SimpleEnantiomerization Mechanism Determination.
Entropy in dissimilarity and chirality measures
Chiral Phosphine−Phosphonium Ylide RhodiumComplexes
Total carbo-Mer of Benzene, Its carbo-Trannulene Form, and theZigzag Nanotube Thereof
Trimesitylmethylphosphonium Cation. SupramolecularStereocontrol and Simple Enantiomerization MechanismDetermination
Chiral Phosphino(sulfinylmethyl)triarylphosphoniumYlide Ligands: Rhodium Complexes and CatalyticProperties
ELF Analysis of Out-of-Plane Aromaticity and In-Plane Homoaromaticity inCarbo[N]annulenes and [N]Pericyclynes
Quantifying the Donor−Acceptor Properties of Carbon Monoxide and Its Carbo-mer Using ELF Analysis
Quadratic Hyperpolarizability of Carbomeric Structures
Novel Cationic Chiral Phosphorus Ligands and TheirZwitterionic Hydridocarbonylferrate Complexes
Diaminocarbene and Phosphonium Ylide Ligands: A Systematic Comparison of their Donor Character
Chemical algebra III: Thermochemical approach to completely G-invariant distances
Chemical algebra. II: Discriminating pairing products
Chemical algebra. IV: “Length” of transformation pathways between skeletal analogs
Chemical algebra. V:G-weighted distance extensions and metrics
Algebra of stereogenic pairing equilibria. 1. General model. 2. Stereoselective reactions under thermodynamic control
Chemical algebra. VII: ImproperG-weighted metrics of non-compact groups: Lorentz group in the Minkowski space
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