Green Synthesis of Pyrrole Derivatives

Autores
Portilla Zúñiga, Omar Miguel; Sathicq, Ángel Gabriel; Martínez Zambrano, José Jobanny; Romanelli, Gustavo Pablo
Año de publicación
2017
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Pyrroles are organic cyclic compounds with an extensive and fascinating chemistry. These compounds have a wide structural variety and are an important basis in technological development as they can be used as drugs, dyes, catalysts, pesticides, etc. Therefore, the production of these heterocyclic compounds by efficient clean methodologies is a great achievement in contemporary chemistry. In this paper, we show recent green procedures in the synthesis of pyrrole derivatives, such as Hantzsch, Knorr and Paal-Knorr syntheses, as well as new eco-friendly synthetic procedures with high efficiency and low environmental impact.
Centro de Investigación y Desarrollo en Ciencias Aplicadas
Materia
Ciencias Exactas
Química
Pyrrole
Green synthesis
Heterocyclic compounds
Hantzsch synthesis
Knorr synthesis
Paal-Knorr synthesis
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-sa/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/104970
Acceder
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repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling Green Synthesis of Pyrrole DerivativesPortilla Zúñiga, Omar MiguelSathicq, Ángel GabrielMartínez Zambrano, José JobannyRomanelli, Gustavo PabloCiencias ExactasQuímicaPyrroleGreen synthesisHeterocyclic compoundsHantzsch synthesisKnorr synthesisPaal-Knorr synthesisPyrroles are organic cyclic compounds with an extensive and fascinating chemistry. These compounds have a wide structural variety and are an important basis in technological development as they can be used as drugs, dyes, catalysts, pesticides, etc. Therefore, the production of these heterocyclic compounds by efficient clean methodologies is a great achievement in contemporary chemistry. In this paper, we show recent green procedures in the synthesis of pyrrole derivatives, such as Hantzsch, Knorr and Paal-Knorr syntheses, as well as new eco-friendly synthetic procedures with high efficiency and low environmental impact.Centro de Investigación y Desarrollo en Ciencias Aplicadas2017info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf1-18http://sedici.unlp.edu.ar/handle/10915/104970enginfo:eu-repo/semantics/altIdentifier/issn/1570-1794info:eu-repo/semantics/altIdentifier/doi/10.2174/1570179414666161206124318info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-10-22T17:03:54Zoai:sedici.unlp.edu.ar:10915/104970Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-10-22 17:03:54.525SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Green Synthesis of Pyrrole Derivatives
title Green Synthesis of Pyrrole Derivatives
spellingShingle Green Synthesis of Pyrrole Derivatives
Portilla Zúñiga, Omar Miguel
Ciencias Exactas
Química
Pyrrole
Green synthesis
Heterocyclic compounds
Hantzsch synthesis
Knorr synthesis
Paal-Knorr synthesis
title_short Green Synthesis of Pyrrole Derivatives
title_full Green Synthesis of Pyrrole Derivatives
title_fullStr Green Synthesis of Pyrrole Derivatives
title_full_unstemmed Green Synthesis of Pyrrole Derivatives
title_sort Green Synthesis of Pyrrole Derivatives
dc.creator.none.fl_str_mv Portilla Zúñiga, Omar Miguel
Sathicq, Ángel Gabriel
Martínez Zambrano, José Jobanny
Romanelli, Gustavo Pablo
author Portilla Zúñiga, Omar Miguel
author_facet Portilla Zúñiga, Omar Miguel
Sathicq, Ángel Gabriel
Martínez Zambrano, José Jobanny
Romanelli, Gustavo Pablo
author_role author
author2 Sathicq, Ángel Gabriel
Martínez Zambrano, José Jobanny
Romanelli, Gustavo Pablo
author2_role author
author
author
dc.subject.none.fl_str_mv Ciencias Exactas
Química
Pyrrole
Green synthesis
Heterocyclic compounds
Hantzsch synthesis
Knorr synthesis
Paal-Knorr synthesis
topic Ciencias Exactas
Química
Pyrrole
Green synthesis
Heterocyclic compounds
Hantzsch synthesis
Knorr synthesis
Paal-Knorr synthesis
dc.description.none.fl_txt_mv Pyrroles are organic cyclic compounds with an extensive and fascinating chemistry. These compounds have a wide structural variety and are an important basis in technological development as they can be used as drugs, dyes, catalysts, pesticides, etc. Therefore, the production of these heterocyclic compounds by efficient clean methodologies is a great achievement in contemporary chemistry. In this paper, we show recent green procedures in the synthesis of pyrrole derivatives, such as Hantzsch, Knorr and Paal-Knorr syntheses, as well as new eco-friendly synthetic procedures with high efficiency and low environmental impact.
Centro de Investigación y Desarrollo en Ciencias Aplicadas
description Pyrroles are organic cyclic compounds with an extensive and fascinating chemistry. These compounds have a wide structural variety and are an important basis in technological development as they can be used as drugs, dyes, catalysts, pesticides, etc. Therefore, the production of these heterocyclic compounds by efficient clean methodologies is a great achievement in contemporary chemistry. In this paper, we show recent green procedures in the synthesis of pyrrole derivatives, such as Hantzsch, Knorr and Paal-Knorr syntheses, as well as new eco-friendly synthetic procedures with high efficiency and low environmental impact.
publishDate 2017
dc.date.none.fl_str_mv 2017
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/10915/104970
url http://sedici.unlp.edu.ar/handle/10915/104970
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/1570-1794
info:eu-repo/semantics/altIdentifier/doi/10.2174/1570179414666161206124318
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
dc.format.none.fl_str_mv application/pdf
1-18
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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