3-ethoxycarbonyl-4-hydroxy-6-(methoxy-methoxy)-1-methyl-2-quinolone

Autores
Pozzi, Gustavo C.; Goeta, Andrés Eduardo; Autino, Juan Carlos; Punte, Graciela María del Carmen
Año de publicación
2003
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
In the title compound, C15H17NO6, the formation of an intramolecular O-H⋯O resonance-assisted hydrogen bond extends the delocalization of the electronic system beyond the two quinoline fused rings.
Facultad de Ciencias Exactas
Materia
Ciencias Exactas
Química
condensation
crystal structure
X ray diffraction analysis
carbocyclic rings
centrosymmetric dimers
hydrogen bonds
aromatic compounds
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/3.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/34644
Acceder
id SEDICI_92b37598c0155695a379f51512f772a1
oai_identifier_str oai:sedici.unlp.edu.ar:10915/34644
network_acronym_str SEDICI
repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling 3-ethoxycarbonyl-4-hydroxy-6-(methoxy-methoxy)-1-methyl-2-quinolonePozzi, Gustavo C.Goeta, Andrés EduardoAutino, Juan CarlosPunte, Graciela María del CarmenCiencias ExactasQuímicacondensationcrystal structureX ray diffraction analysiscarbocyclic ringscentrosymmetric dimershydrogen bondsaromatic compoundsIn the title compound, C15H17NO6, the formation of an intramolecular O-H⋯O resonance-assisted hydrogen bond extends the delocalization of the electronic system beyond the two quinoline fused rings.Facultad de Ciencias Exactas2003-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf1196-1198http://sedici.unlp.edu.ar/handle/10915/34644enginfo:eu-repo/semantics/altIdentifier/url/http://journals.iucr.org/e/issues/2003/08/00/bt6304/bt6304.pdfinfo:eu-repo/semantics/altIdentifier/issn/1600-5368info:eu-repo/semantics/altIdentifier/doi/10.1107/S1600536803016192info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/3.0/Creative Commons Attribution 3.0 Unported (CC BY 3.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-11-12T10:21:52Zoai:sedici.unlp.edu.ar:10915/34644Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-11-12 10:21:52.59SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv 3-ethoxycarbonyl-4-hydroxy-6-(methoxy-methoxy)-1-methyl-2-quinolone
title 3-ethoxycarbonyl-4-hydroxy-6-(methoxy-methoxy)-1-methyl-2-quinolone
spellingShingle 3-ethoxycarbonyl-4-hydroxy-6-(methoxy-methoxy)-1-methyl-2-quinolone
Pozzi, Gustavo C.
Ciencias Exactas
Química
condensation
crystal structure
X ray diffraction analysis
carbocyclic rings
centrosymmetric dimers
hydrogen bonds
aromatic compounds
title_short 3-ethoxycarbonyl-4-hydroxy-6-(methoxy-methoxy)-1-methyl-2-quinolone
title_full 3-ethoxycarbonyl-4-hydroxy-6-(methoxy-methoxy)-1-methyl-2-quinolone
title_fullStr 3-ethoxycarbonyl-4-hydroxy-6-(methoxy-methoxy)-1-methyl-2-quinolone
title_full_unstemmed 3-ethoxycarbonyl-4-hydroxy-6-(methoxy-methoxy)-1-methyl-2-quinolone
title_sort 3-ethoxycarbonyl-4-hydroxy-6-(methoxy-methoxy)-1-methyl-2-quinolone
dc.creator.none.fl_str_mv Pozzi, Gustavo C.
Goeta, Andrés Eduardo
Autino, Juan Carlos
Punte, Graciela María del Carmen
author Pozzi, Gustavo C.
author_facet Pozzi, Gustavo C.
Goeta, Andrés Eduardo
Autino, Juan Carlos
Punte, Graciela María del Carmen
author_role author
author2 Goeta, Andrés Eduardo
Autino, Juan Carlos
Punte, Graciela María del Carmen
author2_role author
author
author
dc.subject.none.fl_str_mv Ciencias Exactas
Química
condensation
crystal structure
X ray diffraction analysis
carbocyclic rings
centrosymmetric dimers
hydrogen bonds
aromatic compounds
topic Ciencias Exactas
Química
condensation
crystal structure
X ray diffraction analysis
carbocyclic rings
centrosymmetric dimers
hydrogen bonds
aromatic compounds
dc.description.none.fl_txt_mv In the title compound, C15H17NO6, the formation of an intramolecular O-H⋯O resonance-assisted hydrogen bond extends the delocalization of the electronic system beyond the two quinoline fused rings.
Facultad de Ciencias Exactas
description In the title compound, C15H17NO6, the formation of an intramolecular O-H⋯O resonance-assisted hydrogen bond extends the delocalization of the electronic system beyond the two quinoline fused rings.
publishDate 2003
dc.date.none.fl_str_mv 2003-07
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
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://sedici.unlp.edu.ar/handle/10915/34644
url http://sedici.unlp.edu.ar/handle/10915/34644
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://journals.iucr.org/e/issues/2003/08/00/bt6304/bt6304.pdf
info:eu-repo/semantics/altIdentifier/issn/1600-5368
info:eu-repo/semantics/altIdentifier/doi/10.1107/S1600536803016192
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/3.0/
Creative Commons Attribution 3.0 Unported (CC BY 3.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/3.0/
Creative Commons Attribution 3.0 Unported (CC BY 3.0)
dc.format.none.fl_str_mv application/pdf
1196-1198
dc.source.none.fl_str_mv reponame:SEDICI (UNLP)
instname:Universidad Nacional de La Plata
instacron:UNLP
reponame_str SEDICI (UNLP)
collection SEDICI (UNLP)
instname_str Universidad Nacional de La Plata
instacron_str UNLP
institution UNLP
repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
repository.mail.fl_str_mv alira@sedici.unlp.edu.ar
_version_ 1848605283802152960
score 13.24909

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