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
- Institución
- Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
- OAI Identificador
- paperaa:paper_14246376_v2000_n4SPECISS_p627_MartinsAlho
Ver los metadatos del registro completo
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paperaa:paper_14246376_v2000_n4SPECISS_p627_MartinsAlho |
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network_name_str |
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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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1846784876598001664 |
score |
12.982451 |