About: Christian Bruneau

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

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) 研究者 (ja) araştırmacı (tr) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) onderzoeker (nl)
rdfs:label	Christian Bruneau (en) Christian Bruneau (es) Christian Bruneau (nl) Christian Bruneau (ast)
skos:prefLabel	Christian Bruneau (en) Christian Bruneau (es) Christian Bruneau (nl) Christian Bruneau (ast)
name	Christian Bruneau (en) Christian Bruneau (es) Christian Bruneau (nl) Christian Bruneau (ast)
Scopus author ID	wds:Q57046929-19B118E2-1150-46F5-9BF5-5A7994C43B8A
Scopus author ID	7007152300
given name	wds:Q57046929-CB31289A-11B8-4720-A47A-8F34451FDC55
given name	Christian
instance of	wds:Q57046929-9A455373-8DE6-4B83-9D00-ED8B0C749774
instance of	Homo sapiens
doctoral student	wds:Q57046929-18F75C7E-B400-417C-A197-CCF6BA938BD1 wds:Q57046929-93C41F03-A3FF-46B1-AB6C-22EFE750DAF4 wds:Q57046929-F38A042D-D708-456E-8263-4163C690BDE2
doctoral student	Hui-Jun Zhang Percia B Arockiam Benoît Liégault
occupation	wds:Q57046929-EC61ADEB-8E52-4B19-90BA-0D2F18402A89
employer	wds:Q57046929-38C179EA-AA3D-4108-B6F4-787D73983B6E
NUKAT ID	wds:Q57046929-78EBF9F4-433D-4916-92F8-0DE544F2E332
sex or gender	wds:Q57046929-F12CE4CA-DEFB-47F8-8843-7A49284DB985
ISNI	wds:Q57046929-41405070-7EE1-493B-ADCB-BB2054A06E8B
VIAF ID	wds:Q57046929-E8C4E20F-9023-4F74-8B7B-97886933B197
GND ID	wds:Q57046929-0e9c2eca-a294-4c8c-b10b-2a4b2a980c46
IdRef ID	wds:Q57046929-958F7617-3645-4F6C-9B94-AD9C9F1FA02D
National Library of Israel J9U ID	wds:Q57046929-C4267E7F-FBB5-487C-8840-6601A6CDB042
VIAF ID	http://viaf.org/viaf/18296690
GND ID	https://d-nb.info/gnd/1229465421
IdRef ID	http://www.idref.fr/069231354/id
occupation	researcher
employer	Délégation Bretagne et Pays de la Loire
NUKAT ID	n2015173889
sex or gender	male
ISNI	0000000042963922
VIAF ID	18296690
GND ID	1229465421
IdRef ID	069231354
National Library of Israel J9U ID	987007363984105171
ORCID iD	wds:Q57046929-07A54031-76AD-428A-8DC7-6C7E2E614CA6
ORCID iD	https://orcid.org/0000-0002-2220-1458
ORCID iD	0000-0002-2220-1458
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57046929
is pr:P3452 of	wdref:effbc9d1df0cd993a25427a7b89a3203eeb1b043
is author of	Ruthenium(II)-catalyzed C-H bond activation and functionalization Ruthenium-catalyzed reductive amination of allylic alcohols Metal vinylidenes and allenylidenes in catalysis: applications in anti-Markovnikov additions to terminal alkynes and alkene metathesis First enantioselective allylic etherification with phenols catalyzed by chiral ruthenium bisoxazoline complexes. Eta6-mesityl,eta1-imidazolinylidene-carbene-ruthenium(II) complexes: catalytic activity of their allenylidene derivatives in alkene metathesis and cycloisomerisation reactions. Synthesis of heteroarylated polyfluorobiphenyls via palladium-catalyzed sequential sp2 C-H bonds functionalizations. Cyclobutene ring-opening of bicyclo[4.2.0]octa-1,6-dienes: access to CF3-substituted 5,6,7,8-tetrahydro-1,7-naphthyridines A new dicoumarinyl ether and two rare furocoumarins from Ruta montana. sp3 C-H bond activation with ruthenium(II) catalysts and C(3)-alkylation of cyclic amines Electrophilic activation and cycloisomerization of enynes: a new route to functional cyclopropanes. A direct route to bifunctional aldehyde derivatives via self- and cross-metathesis of unsaturated aldehydes. Ethenolysis of methyl oleate in room-temperature ionic liquids. Selective ruthenium-catalyzed hydrochlorination of alkynes: one-step synthesis of vinylchlorides Efficient ruthenium-catalyzed synthesis of [3]dendralenes from 1,3-dienic allylic carbonates. Recovery of enlarged olefin metathesis catalysts by nanofiltration in an eco-friendly solvent. Improving sustainability in ene-yne cross-metathesis for transformation of unsaturated fatty esters. Tandem Catalytic Acrylonitrile Cross-Metathesis and Hydrogenation of Nitriles with Ruthenium Catalysts: Direct Access to Linear α,ω-Aminoesters from Renewables Ethenolysis: A Green Catalytic Tool to Cleave Carbon-Carbon Double Bonds. Reactivity of 3-Substituted Fluorobenzenes in Palladium- Catalysed Direct Arylations with Aryl Bromides Ruthenium-catalyzed synthesis of allylic alcohols: boronic acid as a hydroxide source Concomitant monoreduction and hydrogenation of unsaturated cyclic imides to lactams catalyzed by ruthenium compounds Regio- and stereoselective syntheses of piperidine derivatives via ruthenium-catalyzed coupling of propargylic amides and allylic alcohols C-H bond functionalization in water catalyzed by carboxylato ruthenium(II) systems Pentamethylcyclopentadienyl-ruthenium catalysts for regio- and enantioselective allylation of nucleophiles Hydride-induced novel cyclization of dienedinitriles leading to multifunctionalized cyclopentadienes Ruthenium-catalysed synthesis of functional conjugated dienes from propargylic carbonates and silyl diazo compounds Selective and Efficient Iridium Catalyst for the Reductive Amination of Levulinic Acid into Pyrrolidones. C-H Bond Alkylation of Cyclic Amides with Maleimides via a Site-Selective-Determining Six-Membered Ruthenacycle Dimethyl carbonate: an eco-friendly solvent in ruthenium-catalyzed olefin metathesis transformations. Isoquinoline derivatives via stepwise regioselective sp(2) and sp(3) C-H bond functionalizations Iridium-catalyzed oxidant-free dehydrogenative C-H bond functionalization: selective preparation of N-arylpiperidines through tandem hydrogen transfers Ene-yne cross-metathesis with ruthenium carbene catalysts Cp(η2‐bipy)(MeCN)RuIIPF6 Catalysts for Regioselective Allylic Substitution and Characterization of Dicationic Cp(η2‐bipy)(η3‐allyl)RuIVPF62 Intermediates Alkene metathesis catalysis in ionic liquids with ruthenium allenylidene salts. New ruthenium metathesis catalysts with chelating indenylidene ligands: synthesis, characterization and reactivity. Palladium-catalysed direct arylation of thiophenes tolerant to silyl groups

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