About: Emmanuel Lacôte

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

French chemist

Attributes	Values
rdf:type	Item
field of work	wds:Q89178799-4899628B-44FE-48BF-8C56-A9D5E93839C1
field of work	organic chemistry
description	연구원 (ko) 研究者 (ja) French chemist (en) Prantsusmaa keemik (et) chimist francez (ro) kimist francez (sq) químic francès (ca) químico francés (es) químico francés (gl) כימאי צרפתי (he) كيميائي فرنسي (ar) ফরাসি রসায়নবিদ (bn) chimiste français (fr) onderzoeker (nl) Francouzský chemik. Působí na École supérieure de chimie physique électronique de Lyon. (cs)
rdfs:label	Emmanuel Lacôte (cs) Emmanuel Lacôte (en) Emmanuel Lacôte (fr) Emmanuel Lacôte (nl) Emmanuel Lacôte (sk) Emmanuel Lacôte (ast)
skos:prefLabel	Emmanuel Lacôte (cs) Emmanuel Lacôte (en) Emmanuel Lacôte (fr) Emmanuel Lacôte (nl) Emmanuel Lacôte (sk) Emmanuel Lacôte (ast)
name	Emmanuel Lacôte (cs) Emmanuel Lacôte (en) Emmanuel Lacôte (fr) Emmanuel Lacôte (nl) Emmanuel Lacôte (sk) Emmanuel Lacôte (ast)
given name	wds:Q89178799-34FF2BD4-F3AD-4FA0-9A37-02DC4D09620C
given name	Emmanuel
instance of	wds:Q89178799-640026DF-2CF8-4750-86FD-237DDDCC3853
NL CR AUT ID	wds:Q89178799-FA28826D-3EA1-42D5-9DBF-537E261DA049
instance of	Homo sapiens
NL CR AUT ID	ntk2016900041
occupation	wds:Q89178799-2EB57548-F124-4E85-84C8-51522B2FCBE1 wds:Q89178799-FF440676-01A3-48A8-A9A7-6D93D3446E90
NUKAT ID	wds:Q89178799-BA5D7316-752C-4F2D-9E47-6BBC7B9C70DD
languages spoken, written or signed	wds:Q89178799-3FF7F626-5CF0-46C7-B22D-13EFBEBFB426 wds:Q89178799-89BFE538-E975-40A4-B36C-BFBF5A716B28
sex or gender	wds:Q89178799-D2B87746-C750-4847-AAA8-6ADA5B7404D6
ISNI	wds:Q89178799-8C3E3DA0-6493-4984-99B1-D73CC54A2CC5
VIAF ID	wds:Q89178799-2B585990-BFAB-45D3-B96D-EB4497148262 wds:Q89178799-F1DF6297-8B92-4F98-B26E-4E60E49E4C83
IdRef ID	wds:Q89178799-D03D4DD3-4F94-4ABB-B760-D41F9873902A
country of citizenship	wds:Q89178799-1231ffc6-43fa-9937-f239-7852f28f7f06
date of birth	wds:Q89178799-DC57B0E7-6199-4EDD-B4ED-33B564220AD7
educated at	wds:Q89178799-7E19A5CB-22FD-47C1-86A7-F9F88F79393F wds:Q89178799-9D248676-A9E8-485B-9317-28B6EE54F436
family name	wds:Q89178799-B1A2E4EA-9EF1-40EE-9420-31C7D0B8F67D
VIAF ID	http://viaf.org/viaf/193022614 http://viaf.org/viaf/270145541826796601048
IdRef ID	http://www.idref.fr/143360531/id
occupation	researcher chemist
NUKAT ID	n2015069164
languages spoken, written or signed	French English
sex or gender	male
ISNI	000000035705132X
VIAF ID	193022614 270145541826796601048
IdRef ID	143360531
country of citizenship	France
date of birth	1972-01-01 00:00:00Z (xsd:dateTime)
educated at	Stanford University University of Fribourg
family name	Lacôte
ORCID iD	wds:Q89178799-E5692FCC-E507-4AD5-A27F-0209A6624214
ORCID iD	https://orcid.org/0000-0003-0753-6951
ORCID iD	0000-0003-0753-6951
is owl:sameAs of	Emmanuel Lacôte
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q89178799
is author of	Identification of polyoxometalates as nanomolar noncompetitive inhibitors of protein kinase CK2. Recent advances in the use of phosphorus-centered radicals in organic chemistry Radical deoxygenation of xanthates and related functional groups with new minimalist N-heterocyclic carbene boranes Complexes of borane and N-heterocyclic carbenes: a new class of radical hydrogen atom donor Lanthanide polyoxocationic complexes: experimental and theoretical stability studies and Lewis acid catalysis Estimated rate constants for hydrogen abstraction from N-heterocyclic carbene-borane complexes by an alkyl radical Exception to the ortho effect in palladium/norbornene catalysis Synthesis and reactions of N-heterocyclic carbene boranes Substitution reactions at tetracoordinate boron: synthesis of N-heterocyclic carbene boranes with boron-heteroatom bonds Generation and Reactions of an Unsubstituted N-Heterocyclic Carbene Boryl Anion Visible-light-induced photoreductive generation of radicals from epoxides and aziridines Sensing the chirality of Dawson lanthanide polyoxometalates [alpha1-LnP2W17O61]7- by multinuclear NMR spectroscopy Boryltrihydroborate: synthesis, structure, and reactivity as a reductant in ionic, organometallic, and radical reactions N-heterocyclic carbene boryl radicals: a new class of boron-centered radical. Intramolecular homolytic substitution of sulfinates and sulfinamides EPR studies of the generation, structure, and reactivity of n-heterocyclic carbene borane radicals Production and reactions of organic-soluble lanthanide complexes of the monolacunary Dawson [alpha1-P2W17O61]10- polyoxotungstate. Formation of cyclic sulfinates and sulfinamides through homolytic substitution at the sulfur atom Expeditious Synthesis of Phenanthridines from Benzylamines via Dual Palladium Catalysis Water Dissociation on α1-Hafnium and Ytterbium Substituted Dawson Polyoxotungstates: A Density Functional Theory Study†

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