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
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/35119
Acceder
id SEDICI_980a93c42f62f11917b66f8e475f7872
oai_identifier_str oai:sedici.unlp.edu.ar:10915/35119
network_acronym_str SEDICI
repository_id_str 1329
network_name_str SEDICI (UNLP)
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:UNLP2025-10-15T10:49:41Zoai: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:13292025-10-15 10:49:42.263SEDICI (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
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
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score 13.22299

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