Addition of aromatic nucleophiles to a C=N double bond of 1,2,5-thiadiazole 1,1-dioxide
- Autores
- Rozas, M. F.; Piro, Oscar Enrique; Castellano, Eduardo Ernesto; Mirífico, María Virginia; Vasini, Enrique Julio
- Año de publicación
- 2000
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- A new synthesis of 3,4-diphenyl-4-aryl-1,2,5-thiadiazolines 1,1-dioxide through the addition of aromatic derivatives to 1,2,5-thiadiazole 1,1-dioxide is presented. Anhydrous AlCl3 is used as catalyst.
Facultad de Ciencias Exactas - Materia
-
Ciencias Exactas
Química
aromatic compound
carbon
chlorine derivative
nitrogen
oxide
unclassified drug
addition reaction
catalyst
drug synthesis - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by/3.0/
- Repositorio
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/35119
Ver los metadatos del registro completo
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spelling |
Addition of aromatic nucleophiles to a C=N double bond of 1,2,5-thiadiazole 1,1-dioxideRozas, M. F.Piro, Oscar EnriqueCastellano, Eduardo ErnestoMirífico, María VirginiaVasini, Enrique JulioCiencias ExactasQuímicaaromatic compoundcarbonchlorine derivativenitrogenoxideunclassified drugaddition reactioncatalystdrug synthesisA new synthesis of 3,4-diphenyl-4-aryl-1,2,5-thiadiazolines 1,1-dioxide through the addition of aromatic derivatives to 1,2,5-thiadiazole 1,1-dioxide is presented. Anhydrous AlCl3 is used as catalyst.Facultad de Ciencias Exactas2000-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf503-504http://sedici.unlp.edu.ar/handle/10915/35119enginfo:eu-repo/semantics/altIdentifier/url/http://www.mdpi.com/1420-3049/5/3/503info:eu-repo/semantics/altIdentifier/issn/1420-3049info:eu-repo/semantics/altIdentifier/doi/10.3390/50300503info: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:UNLP2025-09-29T10:57:08Zoai:sedici.unlp.edu.ar:10915/35119Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 10:57:09.14SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
Addition of aromatic nucleophiles to a C=N double bond of 1,2,5-thiadiazole 1,1-dioxide |
title |
Addition of aromatic nucleophiles to a C=N double bond of 1,2,5-thiadiazole 1,1-dioxide |
spellingShingle |
Addition of aromatic nucleophiles to a C=N double bond of 1,2,5-thiadiazole 1,1-dioxide Rozas, M. F. Ciencias Exactas Química aromatic compound carbon chlorine derivative nitrogen oxide unclassified drug addition reaction catalyst drug synthesis |
title_short |
Addition of aromatic nucleophiles to a C=N double bond of 1,2,5-thiadiazole 1,1-dioxide |
title_full |
Addition of aromatic nucleophiles to a C=N double bond of 1,2,5-thiadiazole 1,1-dioxide |
title_fullStr |
Addition of aromatic nucleophiles to a C=N double bond of 1,2,5-thiadiazole 1,1-dioxide |
title_full_unstemmed |
Addition of aromatic nucleophiles to a C=N double bond of 1,2,5-thiadiazole 1,1-dioxide |
title_sort |
Addition of aromatic nucleophiles to a C=N double bond of 1,2,5-thiadiazole 1,1-dioxide |
dc.creator.none.fl_str_mv |
Rozas, M. F. Piro, Oscar Enrique Castellano, Eduardo Ernesto Mirífico, María Virginia Vasini, Enrique Julio |
author |
Rozas, M. F. |
author_facet |
Rozas, M. F. Piro, Oscar Enrique Castellano, Eduardo Ernesto Mirífico, María Virginia Vasini, Enrique Julio |
author_role |
author |
author2 |
Piro, Oscar Enrique Castellano, Eduardo Ernesto Mirífico, María Virginia Vasini, Enrique Julio |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
Ciencias Exactas Química aromatic compound carbon chlorine derivative nitrogen oxide unclassified drug addition reaction catalyst drug synthesis |
topic |
Ciencias Exactas Química aromatic compound carbon chlorine derivative nitrogen oxide unclassified drug addition reaction catalyst drug synthesis |
dc.description.none.fl_txt_mv |
A new synthesis of 3,4-diphenyl-4-aryl-1,2,5-thiadiazolines 1,1-dioxide through the addition of aromatic derivatives to 1,2,5-thiadiazole 1,1-dioxide is presented. Anhydrous AlCl3 is used as catalyst. Facultad de Ciencias Exactas |
description |
A new synthesis of 3,4-diphenyl-4-aryl-1,2,5-thiadiazolines 1,1-dioxide through the addition of aromatic derivatives to 1,2,5-thiadiazole 1,1-dioxide is presented. Anhydrous AlCl3 is used as catalyst. |
publishDate |
2000 |
dc.date.none.fl_str_mv |
2000-03 |
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/10915/35119 |
url |
http://sedici.unlp.edu.ar/handle/10915/35119 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/http://www.mdpi.com/1420-3049/5/3/503 info:eu-repo/semantics/altIdentifier/issn/1420-3049 info:eu-repo/semantics/altIdentifier/doi/10.3390/50300503 |
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 503-504 |
dc.source.none.fl_str_mv |
reponame:SEDICI (UNLP) instname:Universidad Nacional de La Plata instacron:UNLP |
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SEDICI (UNLP) - Universidad Nacional de La Plata |
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score |
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