Synthesis and characterization of 2,2-disubstituted thiadiazolines

Autores
Martins Alho, M.A.; Moglioni, A.G.; Brousse, B.; Moltrasio, G.Y.; D'Accorso, N.B.
Año de publicación
2000
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Fil:Martins Alho, M.A. 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 2000;2000(4 SPECISS):627-640
Materia
3,4 dihydronaphthalen 1(2h) one thiosemicarbazone
3,4' dimethoxybenzophenone thiocarbamazone
4 methoxybenzophenone thiocarbamazone
4,4' dimethoxybenzophenone thiocarbamazone
5 acetamido 3 n acetyl 2 (3',4' dimethoxyphenyl) 2 phenyl 1,3,4 thiadiazoline
5 acetamido 3 n acetyl 2 (4' methoxyphenyl) 2 phenyl 1,3,4 thiadiazoline
5 acetamido 3 n acetyl 2,2 bis(4' methoxyphenyl) 1,3,4 thiadiazoline
5 acetamido 3 n acetyl 2,2 diphenyl 1,3 thiadiazoline
5 methoxyindan 1 one thiosemicarbazone
6 methoxyindan 1 one thiosemicarbazone
anthrone thiosemicarbazone
antifungal agent
antiinfective agent
heterocyclic compound
hydrogen
indan 1 one thiosemicarbazone
ketone derivative
spiro[5 acetamido 3 n acetyl 2,1' (1',2',3',4' tetrahydronaphthalen)] 1,3,4 thiadiazoline
spiro[5 acetamido 3 n acetyl 2,1' (5' methoxyindan)] 1,3,4 thiadiazoline
spiro[5 acetamido 3 n acetyl 2,1' (6' methoxyindan)] 1,3,4 thiadiazoline
spiro[5 acetamido 3 n acetyl 2,1' indane] 1,3,4 thiadiazoline
thiadiazole derivative
thiosemicarbazone derivative
unclassified drug
carbon nuclear magnetic resonance
chemical structure
conference paper
drug synthesis
mass spectrometry
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_14246376_v2000_n4SPECISS_p627_MartinsAlho

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oai_identifier_str paperaa:paper_14246376_v2000_n4SPECISS_p627_MartinsAlho
network_acronym_str BDUBAFCEN
repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling Synthesis and characterization of 2,2-disubstituted thiadiazolinesMartins Alho, M.A.Moglioni, A.G.Brousse, B.Moltrasio, G.Y.D'Accorso, N.B.3,4 dihydronaphthalen 1(2h) one thiosemicarbazone3,4' dimethoxybenzophenone thiocarbamazone4 methoxybenzophenone thiocarbamazone4,4' dimethoxybenzophenone thiocarbamazone5 acetamido 3 n acetyl 2 (3',4' dimethoxyphenyl) 2 phenyl 1,3,4 thiadiazoline5 acetamido 3 n acetyl 2 (4' methoxyphenyl) 2 phenyl 1,3,4 thiadiazoline5 acetamido 3 n acetyl 2,2 bis(4' methoxyphenyl) 1,3,4 thiadiazoline5 acetamido 3 n acetyl 2,2 diphenyl 1,3 thiadiazoline5 methoxyindan 1 one thiosemicarbazone6 methoxyindan 1 one thiosemicarbazoneanthrone thiosemicarbazoneantifungal agentantiinfective agentheterocyclic compoundhydrogenindan 1 one thiosemicarbazoneketone derivativespiro[5 acetamido 3 n acetyl 2,1' (1',2',3',4' tetrahydronaphthalen)] 1,3,4 thiadiazolinespiro[5 acetamido 3 n acetyl 2,1' (5' methoxyindan)] 1,3,4 thiadiazolinespiro[5 acetamido 3 n acetyl 2,1' (6' methoxyindan)] 1,3,4 thiadiazolinespiro[5 acetamido 3 n acetyl 2,1' indane] 1,3,4 thiadiazolinethiadiazole derivativethiosemicarbazone derivativeunclassified drugcarbon nuclear magnetic resonancechemical structureconference paperdrug synthesismass spectrometryproton nuclear magnetic resonanceFil:Martins Alho, M.A. 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.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_14246376_v2000_n4SPECISS_p627_MartinsAlhoArkivoc 2000;2000(4 SPECISS):627-640reponame: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/ar2025-10-23T11:18:15Zpaperaa:paper_14246376_v2000_n4SPECISS_p627_MartinsAlhoInstitucionalhttps://digital.bl.fcen.uba.ar/Universidad públicaNo correspondehttps://digital.bl.fcen.uba.ar/cgi-bin/oaiserver.cgiana@bl.fcen.uba.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:18962025-10-23 11:18:17.266Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse
dc.title.none.fl_str_mv Synthesis and characterization of 2,2-disubstituted thiadiazolines
title Synthesis and characterization of 2,2-disubstituted thiadiazolines
spellingShingle Synthesis and characterization of 2,2-disubstituted thiadiazolines
Martins Alho, M.A.
3,4 dihydronaphthalen 1(2h) one thiosemicarbazone
3,4' dimethoxybenzophenone thiocarbamazone
4 methoxybenzophenone thiocarbamazone
4,4' dimethoxybenzophenone thiocarbamazone
5 acetamido 3 n acetyl 2 (3',4' dimethoxyphenyl) 2 phenyl 1,3,4 thiadiazoline
5 acetamido 3 n acetyl 2 (4' methoxyphenyl) 2 phenyl 1,3,4 thiadiazoline
5 acetamido 3 n acetyl 2,2 bis(4' methoxyphenyl) 1,3,4 thiadiazoline
5 acetamido 3 n acetyl 2,2 diphenyl 1,3 thiadiazoline
5 methoxyindan 1 one thiosemicarbazone
6 methoxyindan 1 one thiosemicarbazone
anthrone thiosemicarbazone
antifungal agent
antiinfective agent
heterocyclic compound
hydrogen
indan 1 one thiosemicarbazone
ketone derivative
spiro[5 acetamido 3 n acetyl 2,1' (1',2',3',4' tetrahydronaphthalen)] 1,3,4 thiadiazoline
spiro[5 acetamido 3 n acetyl 2,1' (5' methoxyindan)] 1,3,4 thiadiazoline
spiro[5 acetamido 3 n acetyl 2,1' (6' methoxyindan)] 1,3,4 thiadiazoline
spiro[5 acetamido 3 n acetyl 2,1' indane] 1,3,4 thiadiazoline
thiadiazole derivative
thiosemicarbazone derivative
unclassified drug
carbon nuclear magnetic resonance
chemical structure
conference paper
drug synthesis
mass spectrometry
proton nuclear magnetic resonance
title_short Synthesis and characterization of 2,2-disubstituted thiadiazolines
title_full Synthesis and characterization of 2,2-disubstituted thiadiazolines
title_fullStr Synthesis and characterization of 2,2-disubstituted thiadiazolines
title_full_unstemmed Synthesis and characterization of 2,2-disubstituted thiadiazolines
title_sort Synthesis and characterization of 2,2-disubstituted thiadiazolines
dc.creator.none.fl_str_mv Martins Alho, M.A.
Moglioni, A.G.
Brousse, B.
Moltrasio, G.Y.
D'Accorso, N.B.
author Martins Alho, M.A.
author_facet Martins Alho, M.A.
Moglioni, A.G.
Brousse, B.
Moltrasio, G.Y.
D'Accorso, N.B.
author_role author
author2 Moglioni, A.G.
Brousse, B.
Moltrasio, G.Y.
D'Accorso, N.B.
author2_role author
author
author
author
dc.subject.none.fl_str_mv 3,4 dihydronaphthalen 1(2h) one thiosemicarbazone
3,4' dimethoxybenzophenone thiocarbamazone
4 methoxybenzophenone thiocarbamazone
4,4' dimethoxybenzophenone thiocarbamazone
5 acetamido 3 n acetyl 2 (3',4' dimethoxyphenyl) 2 phenyl 1,3,4 thiadiazoline
5 acetamido 3 n acetyl 2 (4' methoxyphenyl) 2 phenyl 1,3,4 thiadiazoline
5 acetamido 3 n acetyl 2,2 bis(4' methoxyphenyl) 1,3,4 thiadiazoline
5 acetamido 3 n acetyl 2,2 diphenyl 1,3 thiadiazoline
5 methoxyindan 1 one thiosemicarbazone
6 methoxyindan 1 one thiosemicarbazone
anthrone thiosemicarbazone
antifungal agent
antiinfective agent
heterocyclic compound
hydrogen
indan 1 one thiosemicarbazone
ketone derivative
spiro[5 acetamido 3 n acetyl 2,1' (1',2',3',4' tetrahydronaphthalen)] 1,3,4 thiadiazoline
spiro[5 acetamido 3 n acetyl 2,1' (5' methoxyindan)] 1,3,4 thiadiazoline
spiro[5 acetamido 3 n acetyl 2,1' (6' methoxyindan)] 1,3,4 thiadiazoline
spiro[5 acetamido 3 n acetyl 2,1' indane] 1,3,4 thiadiazoline
thiadiazole derivative
thiosemicarbazone derivative
unclassified drug
carbon nuclear magnetic resonance
chemical structure
conference paper
drug synthesis
mass spectrometry
proton nuclear magnetic resonance
topic 3,4 dihydronaphthalen 1(2h) one thiosemicarbazone
3,4' dimethoxybenzophenone thiocarbamazone
4 methoxybenzophenone thiocarbamazone
4,4' dimethoxybenzophenone thiocarbamazone
5 acetamido 3 n acetyl 2 (3',4' dimethoxyphenyl) 2 phenyl 1,3,4 thiadiazoline
5 acetamido 3 n acetyl 2 (4' methoxyphenyl) 2 phenyl 1,3,4 thiadiazoline
5 acetamido 3 n acetyl 2,2 bis(4' methoxyphenyl) 1,3,4 thiadiazoline
5 acetamido 3 n acetyl 2,2 diphenyl 1,3 thiadiazoline
5 methoxyindan 1 one thiosemicarbazone
6 methoxyindan 1 one thiosemicarbazone
anthrone thiosemicarbazone
antifungal agent
antiinfective agent
heterocyclic compound
hydrogen
indan 1 one thiosemicarbazone
ketone derivative
spiro[5 acetamido 3 n acetyl 2,1' (1',2',3',4' tetrahydronaphthalen)] 1,3,4 thiadiazoline
spiro[5 acetamido 3 n acetyl 2,1' (5' methoxyindan)] 1,3,4 thiadiazoline
spiro[5 acetamido 3 n acetyl 2,1' (6' methoxyindan)] 1,3,4 thiadiazoline
spiro[5 acetamido 3 n acetyl 2,1' indane] 1,3,4 thiadiazoline
thiadiazole derivative
thiosemicarbazone derivative
unclassified drug
carbon nuclear magnetic resonance
chemical structure
conference paper
drug synthesis
mass spectrometry
proton nuclear magnetic resonance
dc.description.none.fl_txt_mv Fil:Martins Alho, M.A. 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 Fil:Martins Alho, M.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
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_14246376_v2000_n4SPECISS_p627_MartinsAlho
url http://hdl.handle.net/20.500.12110/paper_14246376_v2000_n4SPECISS_p627_MartinsAlho
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 2000;2000(4 SPECISS):627-640
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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