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
- Institución
- Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
- OAI Identificador
- paperaa:paper_14203049_v5_n3_p418_MartinezEsperon
Ver los metadatos del registro completo
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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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1846142845544562688 |
score |
12.712165 |