About: Laurent El Kaim

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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 # 0000-0001-5729-8010

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) 연구원 (ko) araştırmacı (tr) эрдэмтэн (mn) onderzoeker (nl) researcher, ORCID id # 0000-0001-5729-8010 (en)
rdfs:label	Laurent El Kaim (en) Laurent El Kaim (es) Laurent El Kaim (nl) Laurent El Kaim (ast)
skos:prefLabel	Laurent El Kaim (en) Laurent El Kaim (es) Laurent El Kaim (nl) Laurent El Kaim (ast)
name	Laurent El Kaim (en) Laurent El Kaim (es) Laurent El Kaim (nl) Laurent El Kaim (ast)
Scopus author ID	wds:Q58368802-85CCB60A-1CE7-4D8D-A6C2-1DAAED632821 wds:Q58368802-A66AAC8C-0D54-432A-90E2-F1033EFA9898 wds:Q58368802-C107BAF5-93A2-4CDD-902B-F4A91CF3E1C2
Scopus author ID	10839237900 6508209844 7004017656
given name	wds:Q58368802-BFAEC42A-CCD3-41C9-87AB-68F1BF1B3D3E
given name	Laurent
instance of	wds:Q58368802-25ED75F6-F293-4142-AB24-2C451B94F4AB
instance of	Homo sapiens
doctoral advisor	wds:Q58368802-D699C33C-7D9A-4F42-9645-1598FABD8033
doctoral advisor	Samir Zard
occupation	wds:Q58368802-25EA0A11-0480-4458-BCBD-FCBD5C6F3A1B
sex or gender	wds:Q58368802-8F62B523-6431-48FD-B08D-986F395909A8
ISNI	wds:Q58368802-1F46F344-0E89-465B-8623-294C6D699B92
VIAF ID	wds:Q58368802-E12CA028-4BC1-409D-9F4F-D85F6C55B20E
IdRef ID	wds:Q58368802-B43FA821-2F6C-47F4-8E21-0B7962710C2D
VIAF ID	http://viaf.org/viaf/190755080
IdRef ID	http://www.idref.fr/113678630/id
occupation	researcher
sex or gender	male
ISNI	0000000356623293
VIAF ID	190755080
IdRef ID	113678630
ORCID iD	wds:Q58368802-135744EB-ADC5-458F-A0F0-E07A28C52E10
ORCID iD	https://orcid.org/0000-0001-5729-8010
ORCID iD	0000-0001-5729-8010
HAL author ID	wds:Q58368802-B29F0D1F-21BE-4FE1-869B-7BF8F9C25A78
HAL author ID	laurent-elkaim
ResearcherID	wds:Q58368802-10EE8947-85A2-4B57-9655-7E7E27EB020E
ResearcherID	N-1831-2014
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58368802
is author of	Three-component strategy toward 5-membered heterocycles from isocyanide dibromides N-N bond formation in Ugi processes: from nitric acid to libraries of nitramines Ugi-Smiles couplings: new entries to N-aryl carboxamide derivatives. Selective domino ring-closing metathesis-cross-metathesis reactions between enynes and electron-deficient alkenes Three-component metal-free arylation of isocyanides. Ugi-Smiles couplings of 4-substituted pyridine derivatives: a fast access to chloroquine analogues. Direct Access to Heterocyclic Scaffolds by New Multicomponent Ugi−Smiles Couplings Straightforward four-component access to spiroindolines β-Lactam Synthesis through Diodomethane Addition to Amide Dianions. Palladium catalyzed ring opening of furans as a route to α,β-unsaturated aldehydes Smiles cascades toward heterocyclic scaffolds Correction: Formal [3+2] cycloaddition of Ugi adducts towards pyrrolines. New xanthate-based radical cyclization onto alkynes. Phenol Ugi-Smiles Systems: Strategies for the Multicomponent N-Arylation of Primary Amines with Isocyanides, Aldehydes, and Phenols Xanthate based radical cascade toward multicomponent formation of pyrrolopyrimidines. Predicting new Ugi-smiles couplings: a combined experimental and theoretical study Multicomponent synthesis of fused benzimidazolopiperazines O-arylative Passerini reactions New palladium-catalyzed aerobic oxidative cleavage and cyclization of N-aryl peptide derivatives Formal [3+2] cycloaddition of Ugi adducts towards pyrrolines Evidences for the key role of hydrogen bonds in nucleophilic aromatic substitution reactions Challenging 50 years of established views on Ugi reaction: a theoretical approach Double Smiles rearrangement of Passerini adducts towards benzoxazinones Optimized Conditions for Passerini-Smiles Reactions and Applications to Benzoxazinone Syntheses Isocyanide-based two-step three-component keteneimine formation New ortho-quinone methide formation: application to three-component coupling of isocyanides, aldehydes and phenols Selective Tsuji-Trost type C-allylation of hydrazones: a straightforward entry into 4,5-dihydropyrazoles. Retraction: Predicting New Ugi-Smiles Couplings: A Combined Experimental and Theoretical Study. Substituent effects in Ugi-smiles reactions New Ugi-Smiles-Metathesis Strategy toward the Synthesis of Pyrimido Azepines Pyrrolo[2,3-d]pyrimidine synthesis through activation of N-benzyl groups by distal amides. Straightforward access to complex isoindolinones from the Ugi reaction of o-nitrobenzoic acid derivatives New MCR-Heck-isomerization cascade toward indoles New benzotriazole and benzimidazole scaffolds from Ugi-Smiles couplings of isocyanides Ugi post-condensation copper-triggered oxidative cascade towards pyrazoles. Multiple Roles of Isocyanides in Palladium-Catalyzed Imidoylative Couplings: A Mechanistic Study. First carbamates conversion to amides by simple alkyl group transfer from trialkylalanes New trimethylaluminum-induced mannich-type reaction of hydrazones Propargylation of Ugi Amide Dianion: An Entry into Pyrrolidinone and Benzoindolizidine Alkaloid Analogues. Passerini/Tsuji-Trost strategies towards achieving lactams and cyclopentane derivatives Mannich reaction of trifluoroacetaldehyde hydrazones: a useful entry to trifluoromethyl substituted heterocycles. Palladium triggered diene formation from nitro allylic compounds: a versatile entry into naphthalene derivatives
is author of	wds:Q36263479-1B4E74DE-49D1-458B-85B8-3B534E120C71 wds:Q48351327-0A59C755-FA2E-4D0F-83F7-D7A31489C03F wds:Q46970648-216E65F1-AC35-4674-A433-D478309B622C wds:Q64943211-35BC51C7-7DD0-4773-B776-C72E88C599A6 wds:Q56516918-1C0CFE19-76CD-4BB7-B9E1-41BA2A1E16D2 wds:Q79266678-3E206588-12BA-4DE6-B52A-A29281D7DE5B

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