Behavior of thiosemicarbazones derived from some terpenones under acetylating conditions

Autores
Brousse, B.N.; Moglioni, A.G.; Alho, M.M.; Álvarez-Larena, Á.; Moltrasio, G.Y.; D'Accorso, N.B.
Año de publicación
2002
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Preparation of chiral heterocyclic compounds of the thiadiazoline types, starting from natural terpenones such as fenchone, camphor and menthone, is described. Stereochemical assignment of the compounds synthesized was performed by NMR spectroscopy and X-ray analysis.
Fil:Alho, M.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Moltrasio, G.Y. 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
Arkivoc 2002;2002(10):14-23
Materia
Asymmetric spiro-heterocyclic compounds
Terpenones
Thiadiazolines
Thiosemicarbazones
1,3,3 trimethyl 2 norcamphanone
camphor
heterocyclic compound
menthone
n [aza(1,7,7 trimethylbicyclo[2.2.1]hept 2 ylidene)methyl]acetamide
terpene derivative
thiadiazoline derivative
thiosemicarbazone derivative
unclassified drug
acetylation
article
carbohydrate synthesis
carbon nuclear magnetic resonance
chirality
proton nuclear magnetic resonance
stereochemistry
structure analysis
X ray diffraction
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_14246376_v2002_n10_p14_Brousse
Acceder
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oai_identifier_str paperaa:paper_14246376_v2002_n10_p14_Brousse
network_acronym_str BDUBAFCEN
repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling Behavior of thiosemicarbazones derived from some terpenones under acetylating conditionsBrousse, B.N.Moglioni, A.G.Alho, M.M.Álvarez-Larena, Á.Moltrasio, G.Y.D'Accorso, N.B.Asymmetric spiro-heterocyclic compoundsTerpenonesThiadiazolinesThiosemicarbazones1,3,3 trimethyl 2 norcamphanonecamphorheterocyclic compoundmenthonen [aza(1,7,7 trimethylbicyclo[2.2.1]hept 2 ylidene)methyl]acetamideterpene derivativethiadiazoline derivativethiosemicarbazone derivativeunclassified drugacetylationarticlecarbohydrate synthesiscarbon nuclear magnetic resonancechiralityproton nuclear magnetic resonancestereochemistrystructure analysisX ray diffractionPreparation of chiral heterocyclic compounds of the thiadiazoline types, starting from natural terpenones such as fenchone, camphor and menthone, is described. Stereochemical assignment of the compounds synthesized was performed by NMR spectroscopy and X-ray analysis.Fil:Alho, M.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Moltrasio, G.Y. 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.2002info: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_14246376_v2002_n10_p14_BrousseArkivoc 2002;2002(10):14-23reponame: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/ar2025-10-16T09:30:10Zpaperaa:paper_14246376_v2002_n10_p14_BrousseInstitucionalhttps://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 09:30:12.088Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse
dc.title.none.fl_str_mv Behavior of thiosemicarbazones derived from some terpenones under acetylating conditions
title Behavior of thiosemicarbazones derived from some terpenones under acetylating conditions
spellingShingle Behavior of thiosemicarbazones derived from some terpenones under acetylating conditions
Brousse, B.N.
Asymmetric spiro-heterocyclic compounds
Terpenones
Thiadiazolines
Thiosemicarbazones
1,3,3 trimethyl 2 norcamphanone
camphor
heterocyclic compound
menthone
n [aza(1,7,7 trimethylbicyclo[2.2.1]hept 2 ylidene)methyl]acetamide
terpene derivative
thiadiazoline derivative
thiosemicarbazone derivative
unclassified drug
acetylation
article
carbohydrate synthesis
carbon nuclear magnetic resonance
chirality
proton nuclear magnetic resonance
stereochemistry
structure analysis
X ray diffraction
title_short Behavior of thiosemicarbazones derived from some terpenones under acetylating conditions
title_full Behavior of thiosemicarbazones derived from some terpenones under acetylating conditions
title_fullStr Behavior of thiosemicarbazones derived from some terpenones under acetylating conditions
title_full_unstemmed Behavior of thiosemicarbazones derived from some terpenones under acetylating conditions
title_sort Behavior of thiosemicarbazones derived from some terpenones under acetylating conditions
dc.creator.none.fl_str_mv Brousse, B.N.
Moglioni, A.G.
Alho, M.M.
Álvarez-Larena, Á.
Moltrasio, G.Y.
D'Accorso, N.B.
author Brousse, B.N.
author_facet Brousse, B.N.
Moglioni, A.G.
Alho, M.M.
Álvarez-Larena, Á.
Moltrasio, G.Y.
D'Accorso, N.B.
author_role author
author2 Moglioni, A.G.
Alho, M.M.
Álvarez-Larena, Á.
Moltrasio, G.Y.
D'Accorso, N.B.
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv Asymmetric spiro-heterocyclic compounds
Terpenones
Thiadiazolines
Thiosemicarbazones
1,3,3 trimethyl 2 norcamphanone
camphor
heterocyclic compound
menthone
n [aza(1,7,7 trimethylbicyclo[2.2.1]hept 2 ylidene)methyl]acetamide
terpene derivative
thiadiazoline derivative
thiosemicarbazone derivative
unclassified drug
acetylation
article
carbohydrate synthesis
carbon nuclear magnetic resonance
chirality
proton nuclear magnetic resonance
stereochemistry
structure analysis
X ray diffraction
topic Asymmetric spiro-heterocyclic compounds
Terpenones
Thiadiazolines
Thiosemicarbazones
1,3,3 trimethyl 2 norcamphanone
camphor
heterocyclic compound
menthone
n [aza(1,7,7 trimethylbicyclo[2.2.1]hept 2 ylidene)methyl]acetamide
terpene derivative
thiadiazoline derivative
thiosemicarbazone derivative
unclassified drug
acetylation
article
carbohydrate synthesis
carbon nuclear magnetic resonance
chirality
proton nuclear magnetic resonance
stereochemistry
structure analysis
X ray diffraction
dc.description.none.fl_txt_mv Preparation of chiral heterocyclic compounds of the thiadiazoline types, starting from natural terpenones such as fenchone, camphor and menthone, is described. Stereochemical assignment of the compounds synthesized was performed by NMR spectroscopy and X-ray analysis.
Fil:Alho, M.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Moltrasio, G.Y. 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 Preparation of chiral heterocyclic compounds of the thiadiazoline types, starting from natural terpenones such as fenchone, camphor and menthone, is described. Stereochemical assignment of the compounds synthesized was performed by NMR spectroscopy and X-ray analysis.
publishDate 2002
dc.date.none.fl_str_mv 2002
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_14246376_v2002_n10_p14_Brousse
url http://hdl.handle.net/20.500.12110/paper_14246376_v2002_n10_p14_Brousse
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 Arkivoc 2002;2002(10):14-23
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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score 12.712165

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