Estratégias para a síntese de γ-alquilidenobutenolídeos

Detalhes bibliográficos
Autor(a) principal: Barbosa,Luiz Cláudio Almeida
Data de Publicação: 2010
Outros Autores: Teixeira,Róbson Ricardo, Pinheiro,Patrícia Fontes, Maltha,Célia Regina Álvares, Demuner,Antônio Jacinto
Tipo de documento: Artigo
Idioma: por
Título da fonte: Química Nova (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422010000500030
Resumo: α,β-unsaturated lactones possessing an alkylidene appendage group at the γ-position, are frequently termed γ-alkylidenebutenolides. Over the past decades, an increasing number of these compounds have been isolated from various natural sources. Members of this class of substances vary greatly in structural complexity and functionality. Besides that, many of them have been shown to display a wide range of biological activities. The γ-alkylidenebutenolides has attracted the attention of the organic synthetic chemists resulting in the development of a variety of process to synthesize them. This article review is concerned with the different approaches that can be utilized to prepare γ-alkylidenebutenolides.
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spelling Estratégias para a síntese de γ-alquilidenobutenolídeosγ-alkylidenebutenolidesα,β-unsaturated lactonesbutenolidesα,β-unsaturated lactones possessing an alkylidene appendage group at the γ-position, are frequently termed γ-alkylidenebutenolides. Over the past decades, an increasing number of these compounds have been isolated from various natural sources. Members of this class of substances vary greatly in structural complexity and functionality. Besides that, many of them have been shown to display a wide range of biological activities. The γ-alkylidenebutenolides has attracted the attention of the organic synthetic chemists resulting in the development of a variety of process to synthesize them. This article review is concerned with the different approaches that can be utilized to prepare γ-alkylidenebutenolides.Sociedade Brasileira de Química2010-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422010000500030Química Nova v.33 n.5 2010reponame:Química Nova (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0100-40422010000500030info:eu-repo/semantics/openAccessBarbosa,Luiz Cláudio AlmeidaTeixeira,Róbson RicardoPinheiro,Patrícia FontesMaltha,Célia Regina ÁlvaresDemuner,Antônio Jacintopor2010-08-05T00:00:00Zoai:scielo:S0100-40422010000500030Revistahttps://www.scielo.br/j/qn/ONGhttps://old.scielo.br/oai/scielo-oai.phpquimicanova@sbq.org.br1678-70640100-4042opendoar:2010-08-05T00:00Química Nova (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Estratégias para a síntese de γ-alquilidenobutenolídeos
title Estratégias para a síntese de γ-alquilidenobutenolídeos
spellingShingle Estratégias para a síntese de γ-alquilidenobutenolídeos
Barbosa,Luiz Cláudio Almeida
γ-alkylidenebutenolides
α,β-unsaturated lactones
butenolides
title_short Estratégias para a síntese de γ-alquilidenobutenolídeos
title_full Estratégias para a síntese de γ-alquilidenobutenolídeos
title_fullStr Estratégias para a síntese de γ-alquilidenobutenolídeos
title_full_unstemmed Estratégias para a síntese de γ-alquilidenobutenolídeos
title_sort Estratégias para a síntese de γ-alquilidenobutenolídeos
author Barbosa,Luiz Cláudio Almeida
author_facet Barbosa,Luiz Cláudio Almeida
Teixeira,Róbson Ricardo
Pinheiro,Patrícia Fontes
Maltha,Célia Regina Álvares
Demuner,Antônio Jacinto
author_role author
author2 Teixeira,Róbson Ricardo
Pinheiro,Patrícia Fontes
Maltha,Célia Regina Álvares
Demuner,Antônio Jacinto
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Barbosa,Luiz Cláudio Almeida
Teixeira,Róbson Ricardo
Pinheiro,Patrícia Fontes
Maltha,Célia Regina Álvares
Demuner,Antônio Jacinto
dc.subject.por.fl_str_mv γ-alkylidenebutenolides
α,β-unsaturated lactones
butenolides
topic γ-alkylidenebutenolides
α,β-unsaturated lactones
butenolides
description α,β-unsaturated lactones possessing an alkylidene appendage group at the γ-position, are frequently termed γ-alkylidenebutenolides. Over the past decades, an increasing number of these compounds have been isolated from various natural sources. Members of this class of substances vary greatly in structural complexity and functionality. Besides that, many of them have been shown to display a wide range of biological activities. The γ-alkylidenebutenolides has attracted the attention of the organic synthetic chemists resulting in the development of a variety of process to synthesize them. This article review is concerned with the different approaches that can be utilized to prepare γ-alkylidenebutenolides.
publishDate 2010
dc.date.none.fl_str_mv 2010-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422010000500030
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422010000500030
dc.language.iso.fl_str_mv por
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dc.relation.none.fl_str_mv 10.1590/S0100-40422010000500030
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Química Nova v.33 n.5 2010
reponame:Química Nova (Online)
instname:Sociedade Brasileira de Química (SBQ)
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reponame_str Química Nova (Online)
collection Química Nova (Online)
repository.name.fl_str_mv Química Nova (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv quimicanova@sbq.org.br
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