New spectral data of some flavonoids from Deguelia hatschbachii A.M.G. Azevedo

Detalhes bibliográficos
Autor(a) principal: Magalhães,Aderbal F.
Data de Publicação: 2003
Outros Autores: Tozzi,Ana M. G. A., Magalhães,Eva G., Moraes,Valéria R. de S.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532003000100022
Resumo: From the roots of Deguelia hatschbachii, the known flavonoids scandenin (1), methyl robustate (2) and 4',5- dihydroxy-6-(3,3-dimethylalyll)-7-methoxy flavanone (3) were isolated and characterized by comparison of their spectroscopic data with those found in the literature. Now the inclusion of 1D- and 2D-NMR and MS/MS data has allowed the complete assignment of all hydrogen and carbon chemical shifts in their NMR spectra, as well as the elucidation of the fragmentation pathways of 1-3 in the mass spectrometer.
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spelling New spectral data of some flavonoids from Deguelia hatschbachii A.M.G. AzevedoDeguelia hatschbachiiLeguminosae4-hydroxy-3-phenylcoumarinsflavanoneFrom the roots of Deguelia hatschbachii, the known flavonoids scandenin (1), methyl robustate (2) and 4',5- dihydroxy-6-(3,3-dimethylalyll)-7-methoxy flavanone (3) were isolated and characterized by comparison of their spectroscopic data with those found in the literature. Now the inclusion of 1D- and 2D-NMR and MS/MS data has allowed the complete assignment of all hydrogen and carbon chemical shifts in their NMR spectra, as well as the elucidation of the fragmentation pathways of 1-3 in the mass spectrometer.Sociedade Brasileira de Química2003-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532003000100022Journal of the Brazilian Chemical Society v.14 n.1 2003reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532003000100022info:eu-repo/semantics/openAccessMagalhães,Aderbal F.Tozzi,Ana M. G. A.Magalhães,Eva G.Moraes,Valéria R. de S.eng2003-04-07T00:00:00Zoai:scielo:S0103-50532003000100022Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2003-04-07T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv New spectral data of some flavonoids from Deguelia hatschbachii A.M.G. Azevedo
title New spectral data of some flavonoids from Deguelia hatschbachii A.M.G. Azevedo
spellingShingle New spectral data of some flavonoids from Deguelia hatschbachii A.M.G. Azevedo
Magalhães,Aderbal F.
Deguelia hatschbachii
Leguminosae
4-hydroxy-3-phenylcoumarins
flavanone
title_short New spectral data of some flavonoids from Deguelia hatschbachii A.M.G. Azevedo
title_full New spectral data of some flavonoids from Deguelia hatschbachii A.M.G. Azevedo
title_fullStr New spectral data of some flavonoids from Deguelia hatschbachii A.M.G. Azevedo
title_full_unstemmed New spectral data of some flavonoids from Deguelia hatschbachii A.M.G. Azevedo
title_sort New spectral data of some flavonoids from Deguelia hatschbachii A.M.G. Azevedo
author Magalhães,Aderbal F.
author_facet Magalhães,Aderbal F.
Tozzi,Ana M. G. A.
Magalhães,Eva G.
Moraes,Valéria R. de S.
author_role author
author2 Tozzi,Ana M. G. A.
Magalhães,Eva G.
Moraes,Valéria R. de S.
author2_role author
author
author
dc.contributor.author.fl_str_mv Magalhães,Aderbal F.
Tozzi,Ana M. G. A.
Magalhães,Eva G.
Moraes,Valéria R. de S.
dc.subject.por.fl_str_mv Deguelia hatschbachii
Leguminosae
4-hydroxy-3-phenylcoumarins
flavanone
topic Deguelia hatschbachii
Leguminosae
4-hydroxy-3-phenylcoumarins
flavanone
description From the roots of Deguelia hatschbachii, the known flavonoids scandenin (1), methyl robustate (2) and 4',5- dihydroxy-6-(3,3-dimethylalyll)-7-methoxy flavanone (3) were isolated and characterized by comparison of their spectroscopic data with those found in the literature. Now the inclusion of 1D- and 2D-NMR and MS/MS data has allowed the complete assignment of all hydrogen and carbon chemical shifts in their NMR spectra, as well as the elucidation of the fragmentation pathways of 1-3 in the mass spectrometer.
publishDate 2003
dc.date.none.fl_str_mv 2003-01-01
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=S0103-50532003000100022
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532003000100022
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 Journal of the Brazilian Chemical Society v.14 n.1 2003
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
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collection Journal of the Brazilian Chemical Society (Online)
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repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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