Fatty Acid Esters of Triterpenes from Erythroxylum passerinum

Detalhes bibliográficos
Autor(a) principal: Barreiros,Marizeth L.
Data de Publicação: 2002
Outros Autores: David,Jorge M., Pereira,Pedro A. de P., Guedes,Maria L. S., David,Juceni P.
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=S0103-50532002000500021
Resumo: The hexane extract of leaves of Erythroxylum passerinum yielded besides sitosterol, β-amyrin, lupeol and erythrodiol, β-amyrin palmitate, 3β,28-dihydroxy-olean-12-enyl palmitate, 3β,11β-dihydroxy-olean-12-enyl palmitate, 3β-hydroxy-11-oxo-olean-12-enyl palmitate and 3β-hydroxy-11,12-epoxy-friedoolean-14-enyl palmitate. The structural elucidation of the isolates and of their derivatives were based on spectral data (¹H and 13C NMR, IR and MS).
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spelling Fatty Acid Esters of Triterpenes from Erythroxylum passerinumErythroxylum passerinumErythroxylaceaefatty acid esters of triterpenesThe hexane extract of leaves of Erythroxylum passerinum yielded besides sitosterol, β-amyrin, lupeol and erythrodiol, β-amyrin palmitate, 3β,28-dihydroxy-olean-12-enyl palmitate, 3β,11β-dihydroxy-olean-12-enyl palmitate, 3β-hydroxy-11-oxo-olean-12-enyl palmitate and 3β-hydroxy-11,12-epoxy-friedoolean-14-enyl palmitate. The structural elucidation of the isolates and of their derivatives were based on spectral data (¹H and 13C NMR, IR and MS).Sociedade Brasileira de Química2002-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532002000500021Journal of the Brazilian Chemical Society v.13 n.5 2002reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532002000500021info:eu-repo/semantics/openAccessBarreiros,Marizeth L.David,Jorge M.Pereira,Pedro A. de P.Guedes,Maria L. S.David,Juceni P.eng2008-10-08T00:00:00Zoai:scielo:S0103-50532002000500021Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2008-10-08T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Fatty Acid Esters of Triterpenes from Erythroxylum passerinum
title Fatty Acid Esters of Triterpenes from Erythroxylum passerinum
spellingShingle Fatty Acid Esters of Triterpenes from Erythroxylum passerinum
Barreiros,Marizeth L.
Erythroxylum passerinum
Erythroxylaceae
fatty acid esters of triterpenes
title_short Fatty Acid Esters of Triterpenes from Erythroxylum passerinum
title_full Fatty Acid Esters of Triterpenes from Erythroxylum passerinum
title_fullStr Fatty Acid Esters of Triterpenes from Erythroxylum passerinum
title_full_unstemmed Fatty Acid Esters of Triterpenes from Erythroxylum passerinum
title_sort Fatty Acid Esters of Triterpenes from Erythroxylum passerinum
author Barreiros,Marizeth L.
author_facet Barreiros,Marizeth L.
David,Jorge M.
Pereira,Pedro A. de P.
Guedes,Maria L. S.
David,Juceni P.
author_role author
author2 David,Jorge M.
Pereira,Pedro A. de P.
Guedes,Maria L. S.
David,Juceni P.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Barreiros,Marizeth L.
David,Jorge M.
Pereira,Pedro A. de P.
Guedes,Maria L. S.
David,Juceni P.
dc.subject.por.fl_str_mv Erythroxylum passerinum
Erythroxylaceae
fatty acid esters of triterpenes
topic Erythroxylum passerinum
Erythroxylaceae
fatty acid esters of triterpenes
description The hexane extract of leaves of Erythroxylum passerinum yielded besides sitosterol, β-amyrin, lupeol and erythrodiol, β-amyrin palmitate, 3β,28-dihydroxy-olean-12-enyl palmitate, 3β,11β-dihydroxy-olean-12-enyl palmitate, 3β-hydroxy-11-oxo-olean-12-enyl palmitate and 3β-hydroxy-11,12-epoxy-friedoolean-14-enyl palmitate. The structural elucidation of the isolates and of their derivatives were based on spectral data (¹H and 13C NMR, IR and MS).
publishDate 2002
dc.date.none.fl_str_mv 2002-09-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532002000500021
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532002000500021
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532002000500021
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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.13 n.5 2002
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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