About: Veronique Michelet

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher ORCID ID = 0000-0002-2217-9115

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) araştırmacı (tr) wetenschapper (nl) дослідниця (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) personne médaillée du CNRS (fr) researcher ORCID ID = 0000-0002-2217-9115 (en)
rdfs:label	Veronique Michelet (en) Véronique Michelet (de) Véronique Michelet (es) Véronique Michelet (fr) Véronique Michelet (nl) Véronique Michelet (ast)
skos:prefLabel	Veronique Michelet (en) Véronique Michelet (de) Véronique Michelet (es) Véronique Michelet (fr) Véronique Michelet (nl) Véronique Michelet (ast)
name	Veronique Michelet (en) Véronique Michelet (de) Véronique Michelet (es) Véronique Michelet (fr) Véronique Michelet (nl) Véronique Michelet (ast)
Scopus author ID	wds:Q26875088-febfae85-49c1-1ab6-5427-8e964f66feb8
Scopus author ID	56253704200
given name	wds:Q26875088-9F71CEBD-F3BC-485F-BD08-140DB5B465B5
given name	Véronique
instance of	wds:Q26875088-B9D75EF5-2438-4DAD-87B0-37077CA36E71
described at URL	wds:Q26875088-7A2734FE-DD9D-49AC-8C3E-F16182B5479F
instance of	Homo sapiens
described at URL	https://www.cnrs.fr/fr/personne/veronique-michelet
award received	wds:Q26875088-6C21E227-F7A5-4478-B701-B9BFD8F31AC0
award received	CNRS bronze medal
doctoral student	wds:Q26875088-151DC5BC-E337-4321-A366-676A234F02DF
doctoral student	Alexandre Pradal
skos:altLabel	Véronique Michelet (en)
occupation	wds:Q26875088-8DFBB13A-5654-4A49-ABC2-A56183E801B7
sex or gender	wds:Q26875088-79B59614-9ECE-485A-B890-E3E03D16DA83
VIAF ID	wds:Q26875088-C04F846A-14B6-46A0-B4A6-54A595853B55
IdRef ID	wds:Q26875088-221589C7-DACB-4900-8C64-CFE7A767585A
National Library of Israel J9U ID	wds:Q26875088-80FB68AA-A9ED-40EE-A8AB-ACDCAC8E1F2C
VIAF ID	http://viaf.org/viaf/310717908
IdRef ID	http://www.idref.fr/143151320/id
occupation	researcher
sex or gender	female organism
VIAF ID	310717908
IdRef ID	143151320
National Library of Israel J9U ID	987007354272605171
ORCID iD	wds:Q26875088-45374025-E05A-4C61-9539-4DAE9FCD9287
ORCID iD	https://orcid.org/0000-0002-2217-9115
ORCID iD	0000-0002-2217-9115
CNRS Talent page	wds:Q26875088-0033B84A-DFB5-448C-99FD-B617E23EC520
CNRS Talent page	veronique-michelet
ResearcherID	wds:Q26875088-FF9FCF3A-16B5-4BE2-BA75-C7A0E8DF0574
ResearcherID	A-5601-2009
AcademiaNet ID	wds:Q26875088-210CF01E-E482-4790-AA6D-DAA158FEAE97
AcademiaNet ID	1404087
is owl:sameAs of	Veronique Michelet
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q26875088
is author of	Asymmetric Au-catalyzed cycloisomerization of 1,6-enynes: An entry to bicyclo[4.1.0]heptene Combinatorial approach to chiral tris-ligated carbophilic platinum complexes: application to asymmetric catalysis Synthesis, fluorescence, and two-photon absorption of bidentate phosphane oxide derivatives: complexation with pb(2+) and cd(2+) cations. Highly selective and sensitive phosphane sulfide derivative for the detection of Hg2+ in an organoaqueous medium. Cycloisomerization of 1,n-enynes: challenging metal-catalyzed rearrangements and mechanistic insights. InCl3/CyNH2 cocatalyzed carbocyclization reaction: an entry to α-disubstituted exo-methylene cyclopentanes Combined InCl3- and amine-catalyzed intramolecular addition of alpha-disubstituted aldehydes onto unactivated alkynes Gold-catalyzed hydroamination/cycloisomerization reaction of 1,6-enynes Asymmetric Au(i)-catalyzed synthesis of bicyclo[4.1.0]heptene derivatives via a cycloisomerization process of 1,6-enynes Asymmetric gold-catalyzed hydroarylation/cyclization reactions Asymmetric preparation of polysubstituted cyclopentanes by synergistic Pd(0)/amine catalyzed formal [3+2] cycloadditions of vinyl cyclopropanes with enals. Functionalized carbo- and heterocycles via Pt-catalyzed asymmetric alkoxycyclization of 1,6-enynes Fluorescent phosphane selenide as efficient mercury chemodosimeter. Highly efficient access to strained bicyclic ketals via gold-catalyzed cycloisomerization of bis-homopropargylic diols. Synthesis of novel rod-shaped and star-shaped fluorescent phosphane oxides--nonlinear optical properties and photophysical properties Room temperature Au(I)-catalyzed exo-selective cycloisomerization of acetylenic acids: an entry to functionalized gamma-lactones. Sensitized emission of luminescent lanthanide complexes based on a phosphane oxide derivative. PtCl(2)-catalyzed cycloisomerization of 1,6-enynes for the synthesis of substituted bicyclo[3.1.0]hexanes. Room-temperature Au(I)-catalyzed C-C bond formation through a tandem Friedel-Crafts-type addition/carbocyclization reaction Cycloisomerization of 1,n-enynes via carbophilic activation Efficient metallo-ene reactions in organoaqueous phase Synthesis of Functionalized 1H-Isochromene Derivatives via a Au-Catalyzed Domino Cycloisomerization/Reduction Approach Palladium(0)-Catalyzed Dearomative [3 + 2] Cycloaddition of 3-Nitroindoles with Vinylcyclopropanes: An Entry to Stereodefined 2,3-Fused Cyclopentannulated Indoline Derivatives. One-pot gold-catalyzed aminofluorination of unprotected 2-alkynylanilines. Room-temperature metal-free electrophilic 5-endo-selective iodocarbocyclization of 1,5-enynes. Synthesis, photophysical, and two-photon absorption properties of elongated phosphane oxide and sulfide derivatives. Stereoselective Ir(III)-catalyzed dimerization reaction of enynes: an entry to functionalized polyunsaturated and cyclic systems An IrI-catalyzed exo-selective tandem cycloisomerization/hydroalkoxylation of bis-homopropargylic alcohols at room temperature Mimicking polyolefin carbocyclization reactions: gold-catalyzed intramolecular phenoxycyclization of 1,5-enynes HNTf2-catalyzed regioselective preparation of polysubstituted naphthalene derivatives through alkyne-aldehyde coupling An Original L-shape, Tunable N-Heterocyclic Carbene Platform for Efficient Gold(I) Catalysis Experimental and computational evidence on gold-catalyzed regioselective hydration of phthalimido-protected propargylamines: an entry to β-amino ketones Synthesis of Fluorescent Azafluorenones and Derivatives via a Ruthenium-Catalyzed [2 + 2 + 2] Cycloaddition Chiral undecagold clusters: synthesis, characterization and investigation in catalysis Heterogeneous Gold Catalysts for Efficient Access to Functionalized Lactones

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