Synthesis of β-Arylbutenolides Mediated by BF 3·oMe 2

Detalhes bibliográficos
Autor(a) principal: Finêncio, Beatriz M. [UNESP]
Data de Publicação: 2022
Outros Autores: Santos, Fernanda A. [UNESP], Laurentiz, Rosangela S. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1055/s-0042-1753061
http://hdl.handle.net/11449/247911
Resumo: The reaction of phenols or aryl ethers with tetronic acid mediated by BF3·OMe2 was investigated. This strategy allowed for the preparation of β-(hydroxyaryl)butenolides and β-arylbutenolides in a single step in a simpler way than previously reported synthetic methods.
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spelling Synthesis of β-Arylbutenolides Mediated by BF 3·oMe 2aromatic electrophilic substitutionbutenolidesrubrolidessynthonstetronic acidThe reaction of phenols or aryl ethers with tetronic acid mediated by BF3·OMe2 was investigated. This strategy allowed for the preparation of β-(hydroxyaryl)butenolides and β-arylbutenolides in a single step in a simpler way than previously reported synthetic methods.Universidade Estadual Paulista (Unesp) Faculdade de Engenharia de Ilha Solteira Departamento de Física e Química, SPUniversidade Estadual Paulista (Unesp) Faculdade de Engenharia de Ilha Solteira Departamento de Física e Química, SPUniversidade Estadual Paulista (UNESP)Finêncio, Beatriz M. [UNESP]Santos, Fernanda A. [UNESP]Laurentiz, Rosangela S. [UNESP]2023-07-29T13:29:18Z2023-07-29T13:29:18Z2022-08-26info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article77-80http://dx.doi.org/10.1055/s-0042-1753061Synlett, v. 34, n. 1, p. 77-80, 2022.1437-20960936-5214http://hdl.handle.net/11449/24791110.1055/s-0042-17530612-s2.0-85142205568Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengSynlettinfo:eu-repo/semantics/openAccess2024-07-10T14:07:48Zoai:repositorio.unesp.br:11449/247911Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T19:58:07.657278Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Synthesis of β-Arylbutenolides Mediated by BF 3·oMe 2
title Synthesis of β-Arylbutenolides Mediated by BF 3·oMe 2
spellingShingle Synthesis of β-Arylbutenolides Mediated by BF 3·oMe 2
Finêncio, Beatriz M. [UNESP]
aromatic electrophilic substitution
butenolides
rubrolides
synthons
tetronic acid
title_short Synthesis of β-Arylbutenolides Mediated by BF 3·oMe 2
title_full Synthesis of β-Arylbutenolides Mediated by BF 3·oMe 2
title_fullStr Synthesis of β-Arylbutenolides Mediated by BF 3·oMe 2
title_full_unstemmed Synthesis of β-Arylbutenolides Mediated by BF 3·oMe 2
title_sort Synthesis of β-Arylbutenolides Mediated by BF 3·oMe 2
author Finêncio, Beatriz M. [UNESP]
author_facet Finêncio, Beatriz M. [UNESP]
Santos, Fernanda A. [UNESP]
Laurentiz, Rosangela S. [UNESP]
author_role author
author2 Santos, Fernanda A. [UNESP]
Laurentiz, Rosangela S. [UNESP]
author2_role author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
dc.contributor.author.fl_str_mv Finêncio, Beatriz M. [UNESP]
Santos, Fernanda A. [UNESP]
Laurentiz, Rosangela S. [UNESP]
dc.subject.por.fl_str_mv aromatic electrophilic substitution
butenolides
rubrolides
synthons
tetronic acid
topic aromatic electrophilic substitution
butenolides
rubrolides
synthons
tetronic acid
description The reaction of phenols or aryl ethers with tetronic acid mediated by BF3·OMe2 was investigated. This strategy allowed for the preparation of β-(hydroxyaryl)butenolides and β-arylbutenolides in a single step in a simpler way than previously reported synthetic methods.
publishDate 2022
dc.date.none.fl_str_mv 2022-08-26
2023-07-29T13:29:18Z
2023-07-29T13:29:18Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1055/s-0042-1753061
Synlett, v. 34, n. 1, p. 77-80, 2022.
1437-2096
0936-5214
http://hdl.handle.net/11449/247911
10.1055/s-0042-1753061
2-s2.0-85142205568
url http://dx.doi.org/10.1055/s-0042-1753061
http://hdl.handle.net/11449/247911
identifier_str_mv Synlett, v. 34, n. 1, p. 77-80, 2022.
1437-2096
0936-5214
10.1055/s-0042-1753061
2-s2.0-85142205568
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Synlett
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 77-80
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1808129144649678848

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