About: Gwilherm Evano

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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) वैज्ञानिक (hi) باحت (ary) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) onderzoeker (nl) personne médaillée du CNRS (fr)
rdfs:label	Gwilherm Evano (de) Gwilherm Evano (en) Gwilherm Evano (es) Gwilherm Evano (fr) Gwilherm Evano (nl) Gwilherm Evano (sl) Gwilherm Evano (ast)
skos:prefLabel	Gwilherm Evano (de) Gwilherm Evano (en) Gwilherm Evano (es) Gwilherm Evano (fr) Gwilherm Evano (nl) Gwilherm Evano (sl) Gwilherm Evano (ast)
name	Gwilherm Evano (de) Gwilherm Evano (en) Gwilherm Evano (es) Gwilherm Evano (fr) Gwilherm Evano (nl) Gwilherm Evano (sl) Gwilherm Evano (ast)
given name	wds:Q53326215-7F4F8957-71E7-4788-AF21-33690F0A53CC
given name	Gwilherm
instance of	wds:Q53326215-CD549668-7C6F-434E-8FC9-ABE88A3DE0DA
described at URL	wds:Q53326215-3729AE25-7462-4FA6-8BF8-1735744CB96C
instance of	Homo sapiens
described at URL	https://www.cnrs.fr/fr/personne/gwilherm-evano
award received	wds:Q53326215-40D6DEC4-D920-4FEB-BB2A-D858A8AAFD0E
award received	CNRS bronze medal
Loop ID	wds:Q53326215-EAE3B4D2-345E-449B-8C27-10270060C4DE
Loop ID	457900
occupation	wds:Q53326215-3A4692FA-34D0-44CC-932F-4753E2533014
employer	wds:Q53326215-B1F8DEC8-C13B-4E69-8C8E-C134A4AD6AF2
KBR person ID	wds:Q53326215-7EF3B99D-96B0-4D3C-84CC-6BCDD570C8D7
NUKAT ID	wds:Q53326215-5C29AE85-5D99-4937-AC80-19C026E9D874
sex or gender	wds:Q53326215-BA66FA1E-3A37-4D88-9753-8E61E6D8A908
ISNI	wds:Q53326215-C046CCB4-94BE-4C2A-A402-0C1017FDD66B
VIAF ID	wds:Q53326215-06A09DAD-E175-4A5A-A140-E3A1D6841253
Library of Congress authority ID	wds:Q53326215-5F0BED73-B58F-4097-83EC-FF7855FB4229
IdRef ID	wds:Q53326215-4F08B05F-E895-445F-B35F-660A5E56C6F8
Prabook ID	wds:Q53326215-718C98F0-80B7-4B47-A232-6A240A02011F
date of birth	wds:Q53326215-31B23DCC-4B59-4A49-816A-B0CB4C360665
WorldCat Identities ID (superseded)	wds:Q53326215-C5E74E7E-A134-4E37-BCC9-A213CF8C41F7
National Library of Israel J9U ID	wds:Q53326215-13533C46-51D0-4C01-B292-465FD8895A3E
VIAF ID	http://viaf.org/viaf/213047425
Library of Congress authority ID	http://id.loc.gov/authorities/names/n2013026303
IdRef ID	http://www.idref.fr/070196907/id
occupation	researcher
employer	Free University of Brussels
KBR person ID	14624876
NUKAT ID	n2015054345
sex or gender	male
ISNI	0000000140193925
VIAF ID	213047425
Library of Congress authority ID	n2013026303
IdRef ID	070196907
Prabook ID	183787
date of birth	1977-01-01 00:00:00Z (xsd:dateTime)
WorldCat Identities ID (superseded)	lccn-n2013026303
National Library of Israel J9U ID	987007375906105171
ORCID iD	wds:Q53326215-34B7C326-C129-4913-9E25-8CC8ACCF85DA
ORCID iD	https://orcid.org/0000-0002-2939-4766
ORCID iD	0000-0002-2939-4766
CNRS Talent page	wds:Q53326215-99B10AF8-7C80-4F89-BB80-71FE741426B7
CNRS Talent page	gwilherm-evano
ResearcherID	wds:Q53326215-0EA42DA4-529F-4EC3-AA10-4321D8D43E50
ResearcherID	F-2586-2014
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q53326215
is author of	Copper-mediated coupling reactions and their applications in natural products and designed biomolecules synthesis Total synthesis of the cyclopeptide alkaloid abyssenine A. Application of inter- and intramolecular copper-mediated coupling reactions in organic synthesis Total synthesis of reblastatin Turning unreactive copper acetylides into remarkably powerful and mild alkyne transfer reagents by oxidative umpolung Practical Methods for the Synthesis of Trifluoromethylated Alkynes: Oxidative Trifluoromethylation of Copper Acetylides and Alkynes A convergent synthesis of the macrocyclic core of cytotrienins: application of RCM for macrocyclization. Total synthesis of the cyclopeptide alkaloid paliurine E. insights into macrocyclization by ene--enamide RCM De novo synthesis of 1,4-dihydropyridines and pyridines Total synthesis of chaetominine Impact of copper-catalyzed cross-coupling reactions in natural product synthesis: the emergence of new retrosynthetic paradigms. Stereodivergent Hydrogermylations of α-Trifluoromethylated Alkynes and Their Applications in Cross-Coupling Reactions Azetidinic amino acids: stereocontrolled synthesis and pharmacological characterization as ligands for glutamate receptors and transporters. Copper-catalyzed oxidative alkynylation of diaryl imines with terminal alkynes: a facile synthesis of ynimines Harnessing the Electrophilicity of Keteniminium Ions: A Simple and Straightforward Entry to Tetrahydropyridines and Piperidines from Ynamides. Cationic polycyclization of ynamides: building up molecular complexity. Metal-Mediated Halogen Exchange in Aryl and Vinyl Halides: A Review. A General Copper-Catalyzed Vinylic Halogen Exchange Reaction

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