An alternative synthetic path to 1-substituted 2-naphthol

Autores
Blanco, Guillermo Aldo; Baumgartner, Maria Teresa del V.
Año de publicación
2010
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The photoinduced substitution of the 2-naphthoxide anion was carried out using diethylphosphite, benzenethiolate or 2-naphthalenethiolate anions in the presence of an electron acceptor. The corresponding products were afforded in good yield. This is a simple and convenient approach, which involves the use of 2-naphthol without a leaving group for the synthesis of C1- substituted derivatives.
Fil: Blanco, Guillermo Aldo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
Fil: Baumgartner, Maria Teresa del V.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
Materia
Sinthesys
2-Naphthoxyl Radical
Electron Acceptor
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/69699
Acceder
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repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling An alternative synthetic path to 1-substituted 2-naphtholBlanco, Guillermo AldoBaumgartner, Maria Teresa del V.Sinthesys2-Naphthoxyl RadicalElectron Acceptorhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The photoinduced substitution of the 2-naphthoxide anion was carried out using diethylphosphite, benzenethiolate or 2-naphthalenethiolate anions in the presence of an electron acceptor. The corresponding products were afforded in good yield. This is a simple and convenient approach, which involves the use of 2-naphthol without a leaving group for the synthesis of C1- substituted derivatives.Fil: Blanco, Guillermo Aldo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; ArgentinaFil: Baumgartner, Maria Teresa del V.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; ArgentinaRoyal Society of Chemistry2010-06-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/69699Blanco, Guillermo Aldo; Baumgartner, Maria Teresa del V.; An alternative synthetic path to 1-substituted 2-naphthol; Royal Society of Chemistry; New Journal of Chemistry; 34; 10; 5-6-2010; 2306-23091144-05461369-9261CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/Content/ArticleLanding/2010/NJ/c0nj00265hinfo:eu-repo/semantics/altIdentifier/doi/10.1039/c0nj00265hinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:04:22Zoai:ri.conicet.gov.ar:11336/69699instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:04:22.57CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv An alternative synthetic path to 1-substituted 2-naphthol
title An alternative synthetic path to 1-substituted 2-naphthol
spellingShingle An alternative synthetic path to 1-substituted 2-naphthol
Blanco, Guillermo Aldo
Sinthesys
2-Naphthoxyl Radical
Electron Acceptor
title_short An alternative synthetic path to 1-substituted 2-naphthol
title_full An alternative synthetic path to 1-substituted 2-naphthol
title_fullStr An alternative synthetic path to 1-substituted 2-naphthol
title_full_unstemmed An alternative synthetic path to 1-substituted 2-naphthol
title_sort An alternative synthetic path to 1-substituted 2-naphthol
dc.creator.none.fl_str_mv Blanco, Guillermo Aldo
Baumgartner, Maria Teresa del V.
author Blanco, Guillermo Aldo
author_facet Blanco, Guillermo Aldo
Baumgartner, Maria Teresa del V.
author_role author
author2 Baumgartner, Maria Teresa del V.
author2_role author
dc.subject.none.fl_str_mv Sinthesys
2-Naphthoxyl Radical
Electron Acceptor
topic Sinthesys
2-Naphthoxyl Radical
Electron Acceptor
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The photoinduced substitution of the 2-naphthoxide anion was carried out using diethylphosphite, benzenethiolate or 2-naphthalenethiolate anions in the presence of an electron acceptor. The corresponding products were afforded in good yield. This is a simple and convenient approach, which involves the use of 2-naphthol without a leaving group for the synthesis of C1- substituted derivatives.
Fil: Blanco, Guillermo Aldo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
Fil: Baumgartner, Maria Teresa del V.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
description The photoinduced substitution of the 2-naphthoxide anion was carried out using diethylphosphite, benzenethiolate or 2-naphthalenethiolate anions in the presence of an electron acceptor. The corresponding products were afforded in good yield. This is a simple and convenient approach, which involves the use of 2-naphthol without a leaving group for the synthesis of C1- substituted derivatives.
publishDate 2010
dc.date.none.fl_str_mv 2010-06-05
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/69699
Blanco, Guillermo Aldo; Baumgartner, Maria Teresa del V.; An alternative synthetic path to 1-substituted 2-naphthol; Royal Society of Chemistry; New Journal of Chemistry; 34; 10; 5-6-2010; 2306-2309
1144-0546
1369-9261
CONICET Digital
CONICET
url http://hdl.handle.net/11336/69699
identifier_str_mv Blanco, Guillermo Aldo; Baumgartner, Maria Teresa del V.; An alternative synthetic path to 1-substituted 2-naphthol; Royal Society of Chemistry; New Journal of Chemistry; 34; 10; 5-6-2010; 2306-2309
1144-0546
1369-9261
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/Content/ArticleLanding/2010/NJ/c0nj00265h
info:eu-repo/semantics/altIdentifier/doi/10.1039/c0nj00265h
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
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 reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
_version_ 1844613869160366080
score 13.070432

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