About: Nicolas Duguet

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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) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq)
rdfs:label	Nicolas Duguet (en) Nicolas Duguet (es) Nicolas Duguet (it) Nicolas Duguet (nl) Nicolas Duguet (sl) Nicolas Duguet (ast)
skos:prefLabel	Nicolas Duguet (en) Nicolas Duguet (es) Nicolas Duguet (it) Nicolas Duguet (nl) Nicolas Duguet (sl) Nicolas Duguet (ast)
name	Nicolas Duguet (en) Nicolas Duguet (es) Nicolas Duguet (it) Nicolas Duguet (nl) Nicolas Duguet (sl) Nicolas Duguet (ast)
given name	wds:Q46718011-BC17EDE5-29BB-41F5-BC70-B78582F29FEC
given name	Nicolas
instance of	wds:Q46718011-1D35166C-FFB5-4C5C-9792-6DFADD545E1A
instance of	Homo sapiens
doctoral advisor	wds:Q46718011-16E06251-ACBA-4668-B380-08EA69E5CF90
doctoral advisor	Jacques Maddaluno
occupation	wds:Q46718011-38AB7DF0-8B1A-4088-ADF1-DDB649C13AD9
employer	wds:Q46718011-1C79A425-915B-4ECD-A7DD-84F71FF8C138 wds:Q46718011-84FAAC82-DABA-47BB-B0DD-9CE532ACAAF5 wds:Q46718011-97782F8C-085D-43F5-9479-08E4476D33D4 wds:Q46718011-E9401810-B11C-4AFD-B5E9-DBA403E0318C
sex or gender	wds:Q46718011-A92F9291-8F6D-4102-BE15-F1194837CFC4
VIAF ID	wds:Q46718011-E6F30C97-C21C-4AD7-A0EE-A3D9F7FC4900
IdRef ID	wds:Q46718011-ED255B1A-AC63-4960-B136-0E4B2085A179
family name	wds:Q46718011-602825B8-91E2-4E3F-A382-99E7EC3832EF
VIAF ID	http://viaf.org/viaf/295021930
IdRef ID	http://www.idref.fr/166686549/id
occupation	researcher
employer	Claude Bernard University Lyon 1 University of Orléans University of Rouen University of St Andrews
sex or gender	male
VIAF ID	295021930
IdRef ID	166686549
family name	Duguet
ORCID iD	wds:Q46718011-5FE06664-3D07-4936-AB63-0CC79A12D30B
Dimensions author ID	wds:Q46718011-03C0BB70-8C00-4F9A-BB66-9BA4B8221CD7
ORCID iD	https://orcid.org/0000-0002-9425-7450
ORCID iD	0000-0002-9425-7450
Dimensions author ID	01010121063.06
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q46718011
is author of	Probing the efficiency of N-heterocyclic carbene promoted O- to C-carboxyl transfer of oxazolyl carbonates. N-Heterocyclic carbene catalysed beta-lactam synthesis Enantioselective conjugate addition of a lithium ester enolate catalyzed by chiral lithium amides: a possible intermediate characterized Enantioselective Conjugate Addition of a Lithium Ester Enolate Catalyzed by Chiral Lithium Amides 3-Aminopyrrolidine lithium amides as chiral ligands for alkyllithium derivatives: Synthesis, NMR analysis, and computational study of their mixed aggregates Tandem multi-step synthesis of C-carboxyazlactones promoted by N-heterocyclic carbenes Glycerol Ether Synthesis: A Bench Test for Green Chemistry Concepts and Technologies. Robust organocatalysts for the cleavage of vegetable oil derivatives to aldehydes through retro-benzoin condensation. Heterocyclic lithium amides as chiral ligands for an enantioselective hydroxyalkylation with n-BuLi Origin of the Detrimental Effect of Lithium Halides on an Enantioselective Nucleophilic Alkylation of Aldehydes Asymmetric pericyclic cascade approach to spirocyclic oxindoles Dodecyl sorbitan ethers as antimicrobials against Gram-positive bacteria. Amidation of phenol derivatives: a direct synthesis of paracetamol (acetaminophen) from hydroquinone Structure-enantioselectivity effects in 3,4-dihydropyrimido[2,1-b]benzothiazole-based isothioureas as enantioselective acylation catalysts Identification of New Nonsteroidal RORα Ligands; Related Structure-Activity Relationships and Docking Studies. Synthesis, surfactant properties and antimicrobial activities of methyl glycopyranoside ethers. Dynamics of the Lithium Amide/Alkyllithium Interactions: Mixed Dimers and Beyond Thiazolylidene-catalyzed cleavage of methyl oleate-derived α-hydroxy ketone to the corresponding free aldehydes. An asymmetric hetero-claisen approach to 3-alkyl-3-aryloxindoles An asymmetric pericyclic cascade approach to 3-alkyl-3-aryloxindoles: generality, applications and mechanistic investigations
is author of	wds:Q46463224-9B5342FF-5C03-4D3C-A899-9D0005D8AD6E wds:Q52724121-752A709C-4EBF-4B31-9161-4B05BCCDF016 wds:Q84124547-F85A6039-37ED-4185-AFEC-722D0739430E wds:Q46537297-5B65B5DA-B3E5-4B52-97C9-0884102E2DDB wds:Q50057966-AED5E293-FA15-4D9F-ADF2-98463F89630B wds:Q57959063-C00C8EBC-918C-48A2-9C7B-1EC5EEC254D2 wds:Q39778851-8F655CDD-57D3-4A8E-85C0-6A0AA2CD6B45 wds:Q40347004-EB102502-49C6-4432-8299-9B024E42CB66 wds:Q57958985-AFAE33EF-F2F7-4221-8F9F-1F255F0205D0 wds:Q56113560-D4178209-75A8-4B38-BE8F-6AFF010F0415 wds:Q46223629-D67D3F4C-F263-4D3B-AAF6-7A4EEF634D19 wds:Q38551471-0730E93F-07B7-4A9A-BF53-B9166DE71735 wds:Q52934459-C807C32E-4696-495B-8D7E-FEDD09D7D224 wds:Q57959058-7CB5E013-0B3E-4E7D-B58A-183667359CE5 wds:Q84327124-C7FB7B88-C6CD-4960-AB14-4A780A9D79FE

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