Acylated flavonol glycosides and terpenoids from the leaves of Alibertia sessilis

Detalhes bibliográficos
Autor(a) principal: Olea, RSG
Data de Publicação: 1997
Outros Autores: Roque, N. F., Bolzani, Vanderlan da Silva [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/S0103-50531997000300013
http://hdl.handle.net/11449/35625
Resumo: Two novel acylated flavonol glycosides, along with iridoids, triterpenes, steroids and alpha-tocopherolquinone, were isolated from the leaves of Alibertia sessilis (Rubiaceae). The determination of the structures of the new compounds was based mainly on H-1- and C-13-NMR.
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spelling Acylated flavonol glycosides and terpenoids from the leaves of Alibertia sessilisAlibertia sessilisRubiaceaeacylated flavonol glycosidesiridoidsterpenoidsalpha-tocopherolquinoneTwo novel acylated flavonol glycosides, along with iridoids, triterpenes, steroids and alpha-tocopherolquinone, were isolated from the leaves of Alibertia sessilis (Rubiaceae). The determination of the structures of the new compounds was based mainly on H-1- and C-13-NMR.UNIV SAO PAULO, INST QUIM, BR-05599970 SAO PAULO, SP, BRAZILUNESP, INST QUIM, SAO PAULO, SP, BRAZILUNESP, INST QUIM, SAO PAULO, SP, BRAZILSoc Brasileira QuimicaUniversidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Olea, RSGRoque, N. F.Bolzani, Vanderlan da Silva [UNESP]2014-05-20T15:25:10Z2014-05-20T15:25:10Z1997-05-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article257-259application/pdfhttp://dx.doi.org/10.1590/S0103-50531997000300013Journal of the Brazilian Chemical Society. São Paulo: Soc Brasileira Quimica, v. 8, n. 3, p. 257-259, 1997.0103-5053http://hdl.handle.net/11449/3562510.1590/S0103-50531997000300013S0103-50531997000300013WOS:A1997XG43500013WOSA1997XG43500013.pdf4484083685251673Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of the Brazilian Chemical Society1.4440,357info:eu-repo/semantics/openAccess2024-01-05T06:23:21Zoai:repositorio.unesp.br:11449/35625Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-01-05T06:23:21Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Acylated flavonol glycosides and terpenoids from the leaves of Alibertia sessilis
title Acylated flavonol glycosides and terpenoids from the leaves of Alibertia sessilis
spellingShingle Acylated flavonol glycosides and terpenoids from the leaves of Alibertia sessilis
Olea, RSG
Alibertia sessilis
Rubiaceae
acylated flavonol glycosides
iridoids
terpenoids
alpha-tocopherolquinone
title_short Acylated flavonol glycosides and terpenoids from the leaves of Alibertia sessilis
title_full Acylated flavonol glycosides and terpenoids from the leaves of Alibertia sessilis
title_fullStr Acylated flavonol glycosides and terpenoids from the leaves of Alibertia sessilis
title_full_unstemmed Acylated flavonol glycosides and terpenoids from the leaves of Alibertia sessilis
title_sort Acylated flavonol glycosides and terpenoids from the leaves of Alibertia sessilis
author Olea, RSG
author_facet Olea, RSG
Roque, N. F.
Bolzani, Vanderlan da Silva [UNESP]
author_role author
author2 Roque, N. F.
Bolzani, Vanderlan da Silva [UNESP]
author2_role author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Olea, RSG
Roque, N. F.
Bolzani, Vanderlan da Silva [UNESP]
dc.subject.por.fl_str_mv Alibertia sessilis
Rubiaceae
acylated flavonol glycosides
iridoids
terpenoids
alpha-tocopherolquinone
topic Alibertia sessilis
Rubiaceae
acylated flavonol glycosides
iridoids
terpenoids
alpha-tocopherolquinone
description Two novel acylated flavonol glycosides, along with iridoids, triterpenes, steroids and alpha-tocopherolquinone, were isolated from the leaves of Alibertia sessilis (Rubiaceae). The determination of the structures of the new compounds was based mainly on H-1- and C-13-NMR.
publishDate 1997
dc.date.none.fl_str_mv 1997-05-01
2014-05-20T15:25:10Z
2014-05-20T15:25:10Z
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://dx.doi.org/10.1590/S0103-50531997000300013
Journal of the Brazilian Chemical Society. São Paulo: Soc Brasileira Quimica, v. 8, n. 3, p. 257-259, 1997.
0103-5053
http://hdl.handle.net/11449/35625
10.1590/S0103-50531997000300013
S0103-50531997000300013
WOS:A1997XG43500013
WOSA1997XG43500013.pdf
4484083685251673
url http://dx.doi.org/10.1590/S0103-50531997000300013
http://hdl.handle.net/11449/35625
identifier_str_mv Journal of the Brazilian Chemical Society. São Paulo: Soc Brasileira Quimica, v. 8, n. 3, p. 257-259, 1997.
0103-5053
10.1590/S0103-50531997000300013
S0103-50531997000300013
WOS:A1997XG43500013
WOSA1997XG43500013.pdf
4484083685251673
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of the Brazilian Chemical Society
1.444
0,357
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 257-259
application/pdf
dc.publisher.none.fl_str_mv Soc Brasileira Quimica
publisher.none.fl_str_mv Soc Brasileira Quimica
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1797790207276220416

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