Synthesis of heterocylic compounds of biological interest from carbohydrate derivatives

Autores
Martinez Esperón, M.F.; Fascio, M.L.; D'Accorso, N.B.
Año de publicación
2000
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The synthesis of some isoxazolic compounds from carbohydrate derivatives is described. These products are obtained by 1,3-dipolar cycloaddition reaction and their functionalization leads to derivatives with potential biological activities.
Fil:Fascio, M.L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:D'Accorso, N.B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fuente
Molecules 2000;5(3):418-419
Materia
3 (1',2' o isopropylidene alpha dextro xylofuranos 4' yl) 5 phenyl 2 isoxazole
carbohydrate derivative
heterocyclic compound
isoxazole derivative
unclassified drug
carbon nuclear magnetic resonance
conference paper
cycloaddition
drug activity
drug synthesis
proton nuclear magnetic resonance
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/2.5/ar
Repositorio
Biblioteca Digital (UBA-FCEN)
Institución
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
OAI Identificador
paperaa:paper_14203049_v5_n3_p418_MartinezEsperon

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network_acronym_str BDUBAFCEN
repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling Synthesis of heterocylic compounds of biological interest from carbohydrate derivativesMartinez Esperón, M.F.Fascio, M.L.D'Accorso, N.B.3 (1',2' o isopropylidene alpha dextro xylofuranos 4' yl) 5 phenyl 2 isoxazolecarbohydrate derivativeheterocyclic compoundisoxazole derivativeunclassified drugcarbon nuclear magnetic resonanceconference papercycloadditiondrug activitydrug synthesisproton nuclear magnetic resonanceThe synthesis of some isoxazolic compounds from carbohydrate derivatives is described. These products are obtained by 1,3-dipolar cycloaddition reaction and their functionalization leads to derivatives with potential biological activities.Fil:Fascio, M.L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:D'Accorso, N.B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.2000info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p418_MartinezEsperonMolecules 2000;5(3):418-419reponame:Biblioteca Digital (UBA-FCEN)instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesinstacron:UBA-FCENenginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/2.5/ar2025-10-16T09:30:06Zpaperaa:paper_14203049_v5_n3_p418_MartinezEsperonInstitucionalhttps://digital.bl.fcen.uba.ar/Universidad públicaNo correspondehttps://digital.bl.fcen.uba.ar/cgi-bin/oaiserver.cgiana@bl.fcen.uba.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:18962025-10-16 09:30:08.125Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse
dc.title.none.fl_str_mv Synthesis of heterocylic compounds of biological interest from carbohydrate derivatives
title Synthesis of heterocylic compounds of biological interest from carbohydrate derivatives
spellingShingle Synthesis of heterocylic compounds of biological interest from carbohydrate derivatives
Martinez Esperón, M.F.
3 (1',2' o isopropylidene alpha dextro xylofuranos 4' yl) 5 phenyl 2 isoxazole
carbohydrate derivative
heterocyclic compound
isoxazole derivative
unclassified drug
carbon nuclear magnetic resonance
conference paper
cycloaddition
drug activity
drug synthesis
proton nuclear magnetic resonance
title_short Synthesis of heterocylic compounds of biological interest from carbohydrate derivatives
title_full Synthesis of heterocylic compounds of biological interest from carbohydrate derivatives
title_fullStr Synthesis of heterocylic compounds of biological interest from carbohydrate derivatives
title_full_unstemmed Synthesis of heterocylic compounds of biological interest from carbohydrate derivatives
title_sort Synthesis of heterocylic compounds of biological interest from carbohydrate derivatives
dc.creator.none.fl_str_mv Martinez Esperón, M.F.
Fascio, M.L.
D'Accorso, N.B.
author Martinez Esperón, M.F.
author_facet Martinez Esperón, M.F.
Fascio, M.L.
D'Accorso, N.B.
author_role author
author2 Fascio, M.L.
D'Accorso, N.B.
author2_role author
author
dc.subject.none.fl_str_mv 3 (1',2' o isopropylidene alpha dextro xylofuranos 4' yl) 5 phenyl 2 isoxazole
carbohydrate derivative
heterocyclic compound
isoxazole derivative
unclassified drug
carbon nuclear magnetic resonance
conference paper
cycloaddition
drug activity
drug synthesis
proton nuclear magnetic resonance
topic 3 (1',2' o isopropylidene alpha dextro xylofuranos 4' yl) 5 phenyl 2 isoxazole
carbohydrate derivative
heterocyclic compound
isoxazole derivative
unclassified drug
carbon nuclear magnetic resonance
conference paper
cycloaddition
drug activity
drug synthesis
proton nuclear magnetic resonance
dc.description.none.fl_txt_mv The synthesis of some isoxazolic compounds from carbohydrate derivatives is described. These products are obtained by 1,3-dipolar cycloaddition reaction and their functionalization leads to derivatives with potential biological activities.
Fil:Fascio, M.L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:D'Accorso, N.B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
description The synthesis of some isoxazolic compounds from carbohydrate derivatives is described. These products are obtained by 1,3-dipolar cycloaddition reaction and their functionalization leads to derivatives with potential biological activities.
publishDate 2000
dc.date.none.fl_str_mv 2000
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p418_MartinezEsperon
url http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p418_MartinezEsperon
dc.language.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/2.5/ar
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/2.5/ar
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv Molecules 2000;5(3):418-419
reponame:Biblioteca Digital (UBA-FCEN)
instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN
reponame_str Biblioteca Digital (UBA-FCEN)
collection Biblioteca Digital (UBA-FCEN)
instname_str Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron_str UBA-FCEN
institution UBA-FCEN
repository.name.fl_str_mv Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
repository.mail.fl_str_mv ana@bl.fcen.uba.ar
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