Publicação
Synthesis and transformation of halochromones
| 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). |
|---|---|
| Autores principais: | Tomé, Sara M. |
| Outros Autores: | Silva, Artur; Santos, Clementina M.M. |
| Assunto: | Chromones Cross-coupling reactions Halochromones Halogenation Reactivity Synthesis |
| Ano: | 2014 |
| País: | Portugal |
| Tipo de documento: | artigo |
| Tipo de acesso: | acesso aberto |
| Instituição associada: | Instituto Politécnico de Bragança |
| Idioma: | inglês |
| Origem: | Biblioteca Digital do IPB |
| _version_ | 1867173148091219968 |
|---|---|
| author | Tomé, Sara M. |
| author2 | Silva, Artur Santos, Clementina M.M. |
| author2_role | author author |
| author_facet | Tomé, Sara M. Silva, Artur Santos, Clementina M.M. |
| author_role | author |
| contributor_name_str_mv | Biblioteca Digital do IPB |
| country_str | PT |
| creators_json_txt | [{\"Person.name\":\"Tomé, Sara M.\"},{\"Person.name\":\"Silva, Artur\"},{\"Person.name\":\"Santos, Clementina M.M.\",\"Person.identifier.orcid\":\"0000-0003-4380-7990\"}] |
| datacite.contributors.contributor.contributorName.fl_str_mv | Biblioteca Digital do IPB |
| datacite.creators.creator.creatorName.fl_str_mv | Tomé, Sara M. Silva, Artur Santos, Clementina M.M. |
| datacite.date.Accepted.fl_str_mv | 2014-01-01T00:00:00Z |
| datacite.date.available.fl_str_mv | 2015-03-02T10:31:20Z |
| datacite.date.embargoed.fl_str_mv | 2015-03-02T10:31:20Z |
| datacite.rights.fl_str_mv | http://purl.org/coar/access_right/c_abf2 |
| datacite.subjects.subject.fl_str_mv | Chromones Cross-coupling reactions Halochromones Halogenation Reactivity Synthesis |
| datacite.titles.title.fl_str_mv | Synthesis and transformation of halochromones |
| dc.contributor.none.fl_str_mv | Biblioteca Digital do IPB |
| dc.creator.none.fl_str_mv | Tomé, Sara M. Silva, Artur Santos, Clementina M.M. |
| dc.date.Accepted.fl_str_mv | 2014-01-01T00:00:00Z |
| dc.date.available.fl_str_mv | 2015-03-02T10:31:20Z |
| dc.date.embargoed.fl_str_mv | 2015-03-02T10:31:20Z |
| dc.format.none.fl_str_mv | application/pdf |
| dc.identifier.none.fl_str_mv | http://hdl.handle.net/10198/11714 |
| dc.language.none.fl_str_mv | eng |
| dc.publisher.none.fl_str_mv | Bentham Science |
| dc.rights.none.fl_str_mv | http://purl.org/coar/access_right/c_abf2 |
| dc.subject.none.fl_str_mv | Chromones Cross-coupling reactions Halochromones Halogenation Reactivity Synthesis |
| dc.title.fl_str_mv | Synthesis and transformation of halochromones |
| dc.type.none.fl_str_mv | http://purl.org/coar/resource_type/c_6501 |
| 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). |
| dirty | 0 |
| eu_rights_str_mv | openAccess |
| format | article |
| fulltext.url.fl_str_mv | https://bibliotecadigital.ipb.pt/bitstreams/07121627-2352-4602-867f-10a1f16a8959/download |
| id | ipb_4835f53c8aee8da8bae7ee2044e2fc0b |
| identifier.url.fl_str_mv | http://hdl.handle.net/10198/11714 |
| instacron_str | ipb |
| institution | Instituto Politécnico de Bragança |
| instname_str | Instituto Politécnico de Bragança |
| language | eng |
| network_acronym_str | ipb |
| network_name_str | Biblioteca Digital do IPB |
| oai_identifier_str | oai:bibliotecadigital.ipb.pt:10198/11714 |
| organization_str_mv | urn:organizationAcronym:ipb |
| person_str_mv | Tomé, Sara M. Silva, Artur Santos, Clementina M.M. Santos, Clementina M.M. https://www.ciencia-id.pt/9018-DB9C-C590 9018-DB9C-C590 http://orcid.org/0000-0003-4380-7990 0000-0003-4380-7990 |
| publishDate | 2014 |
| publisher.none.fl_str_mv | Bentham Science |
| reponame_str | Biblioteca Digital do IPB |
| repository_id_str | urn:repositoryAcronym:ipb |
| service_str_mv | urn:repositoryAcronym:ipb |
| spelling | engBentham ScienceporChromones (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).application/pdfporSynthesis and transformation of halochromonesTomé, Sara M.Silva, ArturPersonalSantos, Clementina M.M.DSpacehttp://dspace.org/items/64f662b6-775d-4ea0-bfd7-f527af0ac1a0DSpacehttp://dspace.org/items/64f662b6-775d-4ea0-bfd7-f527af0ac1a0SantosClementina M.M.Ciência IDhttps://www.ciencia-id.pt9018-DB9C-C590ORCIDhttp://orcid.org0000-0003-4380-7990Scopus Author IDhttps://www.scopus.com7201458663HostingInstitutionOrganizationalBiblioteca Digital do IPBe-mailmailto:dspace@ipb.ptdspace@ipb.ptISSNIsPartOf1570-1794DOIIsPartOf10.2174/157017941131099900632015-03-02T10:31:20Z20142014-01-01T00:00:00ZHandlehttp://hdl.handle.net/10198/11714http://purl.org/coar/access_right/c_abf2open accessChromonesCross-coupling reactionsHalochromonesHalogenationReactivitySynthesis610661 bytesliteraturehttp://purl.org/coar/resource_type/c_6501journal articlehttp://purl.org/coar/access_right/c_abf2application/pdffulltexthttps://bibliotecadigital.ipb.pt/bitstreams/07121627-2352-4602-867f-10a1f16a8959/downloadCurr. Org. Synth.11317341 |
| spellingShingle | Synthesis and transformation of halochromones Tomé, Sara M. Chromones Cross-coupling reactions Halochromones Halogenation Reactivity Synthesis |
| status | SINGLETON |
| subject.fl_str_mv | Chromones Cross-coupling reactions Halochromones Halogenation Reactivity Synthesis |
| title | 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_short | Synthesis and transformation of halochromones |
| title_sort | Synthesis and transformation of halochromones |
| topic | Chromones Cross-coupling reactions Halochromones Halogenation Reactivity Synthesis |
| topic_facet | Chromones Cross-coupling reactions Halochromones Halogenation Reactivity Synthesis |
| url | http://hdl.handle.net/10198/11714 |
| visible | 1 |