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http://hub.abes.fr/bmj/periodical/gutjnl/2002/volume_50/issue_3/B356B02520E73CE9E053120B220A6533/authorship/9
http://hub.abes.fr/acs/periodical/joceah/1985/volume_50/issue_23/101021jo00223a005/authorship/5
http://hub.abes.fr/acs/periodical/joceah/1988/volume_53/issue_8/101021jo00243a002/authorship/4
http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_26/101021jo026068/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1997/volume_62/issue_24/101021jo9708607/authorship/5
http://hub.abes.fr/acs/periodical/orgnd7/2006/volume_25/issue_17/101021om060606h/authorship/5
http://hub.abes.fr/acs/periodical/joceah/2006/volume_71/issue_19/101021jo061359u/authorship/4
http://hub.abes.fr/acs/periodical/orgnd7/2007/volume_26/issue_2/101021om060846x/authorship/5
http://hub.abes.fr/acs/periodical/orgnd7/2003/volume_22/issue_9/101021om030066d/authorship/5
http://hub.abes.fr/acs/periodical/joceah/1998/volume_63/issue_26/101021jo981599c/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1999/volume_64/issue_8/101021jo982266i/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1998/volume_63/issue_3/101021jo971849/authorship/4
http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_15/101021jo800707q/authorship/6
http://hub.abes.fr/acs/periodical/joceah/1987/volume_52/issue_24/101021jo00233a028/authorship/3
http://hub.abes.fr/acs/periodical/joceah/1991/volume_56/issue_25/101021jo00025a001/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1986/volume_51/issue_25/101021jo00375a064/authorship/3
http://hub.abes.fr/acs/periodical/joceah/1993/volume_58/issue_11/101021jo00063a044/authorship/1
http://hub.abes.fr/springer/periodical/10616/1993/volume_11/issue_1/B9116E0A87D532E5E053120B220AB819/authorship/1
http://hub.abes.fr/springer/periodical/10616/1993/volume_11/issue_1/B9116E0A87DA32E5E053120B220AB819/authorship/6
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Addition of racemic alkoxyallylstannanes to an enantiomerically pure 2-methoxyoxazolidine: an example of combined mutual diastereoface selection and kinetic resolution
Synthetic opportunities offered by anti .alpha.-methylene-.beta.-hydroxy-.gamma.-alkoxy esters: stereoselective reactions at the double bond
Allylic stereocenter directed asymmetric conjugate addition. Enantioselective synthesis of 3-alkylsuccinaldehydic acid methyl esters
Absolute configuration of A-32'287 [conocandin] and total synthesis of its methyl and tert-butyl esters
Palladium-Catalyzed Allylic Alkylations viaTitanated Nucleophiles: A New Early−LateHeterobimetallic System
Oxidative Addition of Ligand-Chelated Palladium(0) to ArylHalides: Comparison between 1,2-Bisthioethers and1,2-Bisphosphines
A Selective Access to Amino HydroxyOxetanes
Rationalizing Ring-Size Selectivity in IntramolecularPd-Catalyzed Allylations of Resonance-StabilizedCarbanions
An Epiisopicropodophyllin Aza Analoguevia Palladium-Catalyzed Pseudo-DominoCyclization
New Picropodophyllin Analogs via Palladium-Catalyzed Allylic Alkylation−Hiyama Cross-Coupling Sequences
Preparation of Allyl Sulfoxides by Palladium-Catalyzed AllylicAlkylation of Sulfenate Anions
Rationalizing Ring-Size Selectivity in Intramolecular Pd-Catalyzed Allylations ofResonance-Stabilized Carbanions
Palladium Catalyzed Alkylation with AllylicAcetates under Neutral Conditions
A New Palladium-Catalyzed Intramolecular Allylation toPyrrolidin-2-ones1
Lipid peroxidation in hepatoma cell lines and their sensitivity to 4-hydroxynonenal
The first asymmetric synthesis of enantiopure .alpha.-sulfenyl dithioacetals and .alpha.-sulfenyl aldehydes
Norephedrine-derived 2-alkenyloxazolidines: stereochemistry of cyclization and allylic stereocenter directed asymmetric conjugate addition
Rat hepatocytes in single cell suspension: A still suitable system for lipid peroxidation studies
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