Palladium-catalysed intramolecular carbenoid insertion of α-diazo α-(methoxycarbonyl)acetanilides for oxindole synthesis

A novel, selective palladium-catalysed carbenoid C(aryl)-H insertion of α-diazo-α-(methoxycarbonyl)acetanilides leading to oxindoles is described.

Detalles Bibliográficos
Autores: Solé Arjó, Daniel, Pérez Janer, Ferran, Fernández Cadenas, Israel
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2017
País:España
Institución:Universidad de Barcelona
Repositorio:Dipòsit Digital de la UB
OAI Identifier:oai:diposit.ub.edu:2445/127839
Acceso en línea:https://hdl.handle.net/2445/127839
Access Level:acceso abierto
Palabra clave:Pal·ladi (Element químic)
Catàlisi
Síntesi orgànica
Carbens
Palladium
Catalysis
Organic synthesis
Carbenes
id ES_28abb02ca3ed830d58de8b442f6eb070
oai_identifier_str oai:diposit.ub.edu:2445/127839
network_acronym_str ES
network_name_str España
repository_id_str
spelling Palladium-catalysed intramolecular carbenoid insertion of α-diazo α-(methoxycarbonyl)acetanilides for oxindole synthesisSolé Arjó, DanielPérez Janer, FerranFernández Cadenas, IsraelPal·ladi (Element químic)CatàlisiSíntesi orgànicaCarbensPalladiumCatalysisOrganic synthesisCarbenesA novel, selective palladium-catalysed carbenoid C(aryl)-H insertion of α-diazo-α-(methoxycarbonyl)acetanilides leading to oxindoles is described.Royal Society of Chemistry2017info:eu-repo/semantics/articleinfo:eu-repo/semantics/acceptedVersionapplication/pdfhttps://hdl.handle.net/2445/127839Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)reponame:Dipòsit Digital de la UBinstname:Universidad de BarcelonaInglésVersió postprint del document publicat a: https://doi.org/10.1039/c7cc00718cChemical Communications, 2017, vol. 53, num. 21, p. 3110-3113https://doi.org/10.1039/c7cc00718c(c) Solé Arjó, Daniel et al., 2017info:eu-repo/semantics/openAccessoai:diposit.ub.edu:2445/1278392026-05-27T06:46:51Z
dc.title.none.fl_str_mv Palladium-catalysed intramolecular carbenoid insertion of α-diazo α-(methoxycarbonyl)acetanilides for oxindole synthesis
title Palladium-catalysed intramolecular carbenoid insertion of α-diazo α-(methoxycarbonyl)acetanilides for oxindole synthesis
spellingShingle Palladium-catalysed intramolecular carbenoid insertion of α-diazo α-(methoxycarbonyl)acetanilides for oxindole synthesis
Solé Arjó, Daniel
Pal·ladi (Element químic)
Catàlisi
Síntesi orgànica
Carbens
Palladium
Catalysis
Organic synthesis
Carbenes
title_short Palladium-catalysed intramolecular carbenoid insertion of α-diazo α-(methoxycarbonyl)acetanilides for oxindole synthesis
title_full Palladium-catalysed intramolecular carbenoid insertion of α-diazo α-(methoxycarbonyl)acetanilides for oxindole synthesis
title_fullStr Palladium-catalysed intramolecular carbenoid insertion of α-diazo α-(methoxycarbonyl)acetanilides for oxindole synthesis
title_full_unstemmed Palladium-catalysed intramolecular carbenoid insertion of α-diazo α-(methoxycarbonyl)acetanilides for oxindole synthesis
title_sort Palladium-catalysed intramolecular carbenoid insertion of α-diazo α-(methoxycarbonyl)acetanilides for oxindole synthesis
dc.creator.none.fl_str_mv Solé Arjó, Daniel
Pérez Janer, Ferran
Fernández Cadenas, Israel
author Solé Arjó, Daniel
author_facet Solé Arjó, Daniel
Pérez Janer, Ferran
Fernández Cadenas, Israel
author_role author
author2 Pérez Janer, Ferran
Fernández Cadenas, Israel
author2_role author
author
dc.subject.none.fl_str_mv Pal·ladi (Element químic)
Catàlisi
Síntesi orgànica
Carbens
Palladium
Catalysis
Organic synthesis
Carbenes
topic Pal·ladi (Element químic)
Catàlisi
Síntesi orgànica
Carbens
Palladium
Catalysis
Organic synthesis
Carbenes
description A novel, selective palladium-catalysed carbenoid C(aryl)-H insertion of α-diazo-α-(methoxycarbonyl)acetanilides leading to oxindoles is described.
publishDate 2017
dc.date.none.fl_str_mv 2017
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/acceptedVersion
format article
status_str acceptedVersion
dc.identifier.none.fl_str_mv https://hdl.handle.net/2445/127839
url https://hdl.handle.net/2445/127839
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.relation.none.fl_str_mv Versió postprint del document publicat a: https://doi.org/10.1039/c7cc00718c
Chemical Communications, 2017, vol. 53, num. 21, p. 3110-3113
https://doi.org/10.1039/c7cc00718c
dc.rights.none.fl_str_mv (c) Solé Arjó, Daniel et al., 2017
info:eu-repo/semantics/openAccess
rights_invalid_str_mv (c) Solé Arjó, Daniel et al., 2017
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Royal Society of Chemistry
publisher.none.fl_str_mv Royal Society of Chemistry
dc.source.none.fl_str_mv Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)
reponame:Dipòsit Digital de la UB
instname:Universidad de Barcelona
instname_str Universidad de Barcelona
reponame_str Dipòsit Digital de la UB
collection Dipòsit Digital de la UB
repository.name.fl_str_mv
repository.mail.fl_str_mv
_version_ 1869404959350456320
score 15,300724

Similares en LA Referencia