Synthesis and transformation of halochromones

Detalhes bibliográficos
Autor(a) principal: Tomé, Sara M.
Data de Publicação: 2014
Outros Autores: Silva, Artur, Santos, Clementina M.M.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10198/11714
Resumo: Chromones (4H-1-benzopyran-4-ones) are one of the most abundant groups of naturally occurring oxygen containing heterocyclic compounds possessing a benzo-γ-pyrone framework, 1a. The significance of these widely spread and highly diverse compounds is far beyond the important biological functions they assume in nature [1, 2]. Natural and synthetic chromone derivatives have been assigned as lead structures in drug development with some already being marketed [3]. The majority of the naturally occurring chromones are 2- and 3-aryl derivatives, called flavones 1b and isoflavones 1c, respectively. However, other types of chromones have also been found in the plant kingdom, such as 3-methylchromones 1d and 2- styrylchromones 1e (Fig. 1).
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spelling Synthesis and transformation of halochromonesChromonesCross-coupling reactionsHalochromonesHalogenationReactivitySynthesisChromones (4H-1-benzopyran-4-ones) are one of the most abundant groups of naturally occurring oxygen containing heterocyclic compounds possessing a benzo-γ-pyrone framework, 1a. The significance of these widely spread and highly diverse compounds is far beyond the important biological functions they assume in nature [1, 2]. Natural and synthetic chromone derivatives have been assigned as lead structures in drug development with some already being marketed [3]. The majority of the naturally occurring chromones are 2- and 3-aryl derivatives, called flavones 1b and isoflavones 1c, respectively. However, other types of chromones have also been found in the plant kingdom, such as 3-methylchromones 1d and 2- styrylchromones 1e (Fig. 1).University of Aveiro, Fundação para a Ciência e a Tecnologia (FCT, Portugal), European Union, QREN, FEDER and COMPETE for funding the QOPNA Research Unit.Bentham ScienceBiblioteca Digital do IPBTomé, Sara M.Silva, ArturSantos, Clementina M.M.2015-03-02T10:31:20Z20142014-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10198/11714engTomé, Sara M.; Silva, Artur M.S.; Santos, Clementina M.M. (2014). Synthesis and transformation of halochromones. Current Organic Synthesis. ISSN 1570-1794. 11:3, p. 317-3411570-179410.2174/15701794113109990063info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-21T10:27:28Zoai:bibliotecadigital.ipb.pt:10198/11714Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T23:02:10.290101Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Synthesis and transformation of halochromones
title Synthesis and transformation of halochromones
spellingShingle Synthesis and transformation of halochromones
Tomé, Sara M.
Chromones
Cross-coupling reactions
Halochromones
Halogenation
Reactivity
Synthesis
title_short Synthesis and transformation of halochromones
title_full Synthesis and transformation of halochromones
title_fullStr Synthesis and transformation of halochromones
title_full_unstemmed Synthesis and transformation of halochromones
title_sort Synthesis and transformation of halochromones
author Tomé, Sara M.
author_facet Tomé, Sara M.
Silva, Artur
Santos, Clementina M.M.
author_role author
author2 Silva, Artur
Santos, Clementina M.M.
author2_role author
author
dc.contributor.none.fl_str_mv Biblioteca Digital do IPB
dc.contributor.author.fl_str_mv Tomé, Sara M.
Silva, Artur
Santos, Clementina M.M.
dc.subject.por.fl_str_mv Chromones
Cross-coupling reactions
Halochromones
Halogenation
Reactivity
Synthesis
topic Chromones
Cross-coupling reactions
Halochromones
Halogenation
Reactivity
Synthesis
description Chromones (4H-1-benzopyran-4-ones) are one of the most abundant groups of naturally occurring oxygen containing heterocyclic compounds possessing a benzo-γ-pyrone framework, 1a. The significance of these widely spread and highly diverse compounds is far beyond the important biological functions they assume in nature [1, 2]. Natural and synthetic chromone derivatives have been assigned as lead structures in drug development with some already being marketed [3]. The majority of the naturally occurring chromones are 2- and 3-aryl derivatives, called flavones 1b and isoflavones 1c, respectively. However, other types of chromones have also been found in the plant kingdom, such as 3-methylchromones 1d and 2- styrylchromones 1e (Fig. 1).
publishDate 2014
dc.date.none.fl_str_mv 2014
2014-01-01T00:00:00Z
2015-03-02T10:31:20Z
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://hdl.handle.net/10198/11714
url http://hdl.handle.net/10198/11714
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Tomé, Sara M.; Silva, Artur M.S.; Santos, Clementina M.M. (2014). Synthesis and transformation of halochromones. Current Organic Synthesis. ISSN 1570-1794. 11:3, p. 317-341
1570-1794
10.2174/15701794113109990063
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.publisher.none.fl_str_mv Bentham Science
publisher.none.fl_str_mv Bentham Science
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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