Ionic liquid catalyzed convenient synthesis of imidazo[1,2-a]quinoline under sonic condition

Detalhes bibliográficos
Autor(a) principal: Patel,Devji S.
Data de Publicação: 2012
Outros Autores: Avalani,Jemin R., Raval,Dipak K.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012001000026
Resumo: An efficient protocol for the synthesis of imidazo[1,2-a]quinoline from aldehydes, enaminones, and malononitrile using 1,8-diazabicyclo[5.4.0]-undec-7-en-8-ium acetate ([DBU][Ac]) as a catalyst under ultrasound irradiation is described. Compared with other methods, this new method has the advantages of easier work-up, milder reaction conditions, high yields and environmentally benign procedure.
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spelling Ionic liquid catalyzed convenient synthesis of imidazo[1,2-a]quinoline under sonic conditionionic liquidimidazo[1,2-a]quinoline([DBU][Ac])green catalystmulticomponent reactionone pot synthesisAn efficient protocol for the synthesis of imidazo[1,2-a]quinoline from aldehydes, enaminones, and malononitrile using 1,8-diazabicyclo[5.4.0]-undec-7-en-8-ium acetate ([DBU][Ac]) as a catalyst under ultrasound irradiation is described. Compared with other methods, this new method has the advantages of easier work-up, milder reaction conditions, high yields and environmentally benign procedure.Sociedade Brasileira de Química2012-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012001000026Journal of the Brazilian Chemical Society v.23 n.10 2012reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532012005000051info:eu-repo/semantics/openAccessPatel,Devji S.Avalani,Jemin R.Raval,Dipak K.eng2012-12-05T00:00:00Zoai:scielo:S0103-50532012001000026Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2012-12-05T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Ionic liquid catalyzed convenient synthesis of imidazo[1,2-a]quinoline under sonic condition
title Ionic liquid catalyzed convenient synthesis of imidazo[1,2-a]quinoline under sonic condition
spellingShingle Ionic liquid catalyzed convenient synthesis of imidazo[1,2-a]quinoline under sonic condition
Patel,Devji S.
ionic liquid
imidazo[1,2-a]quinoline
([DBU][Ac])
green catalyst
multicomponent reaction
one pot synthesis
title_short Ionic liquid catalyzed convenient synthesis of imidazo[1,2-a]quinoline under sonic condition
title_full Ionic liquid catalyzed convenient synthesis of imidazo[1,2-a]quinoline under sonic condition
title_fullStr Ionic liquid catalyzed convenient synthesis of imidazo[1,2-a]quinoline under sonic condition
title_full_unstemmed Ionic liquid catalyzed convenient synthesis of imidazo[1,2-a]quinoline under sonic condition
title_sort Ionic liquid catalyzed convenient synthesis of imidazo[1,2-a]quinoline under sonic condition
author Patel,Devji S.
author_facet Patel,Devji S.
Avalani,Jemin R.
Raval,Dipak K.
author_role author
author2 Avalani,Jemin R.
Raval,Dipak K.
author2_role author
author
dc.contributor.author.fl_str_mv Patel,Devji S.
Avalani,Jemin R.
Raval,Dipak K.
dc.subject.por.fl_str_mv ionic liquid
imidazo[1,2-a]quinoline
([DBU][Ac])
green catalyst
multicomponent reaction
one pot synthesis
topic ionic liquid
imidazo[1,2-a]quinoline
([DBU][Ac])
green catalyst
multicomponent reaction
one pot synthesis
description An efficient protocol for the synthesis of imidazo[1,2-a]quinoline from aldehydes, enaminones, and malononitrile using 1,8-diazabicyclo[5.4.0]-undec-7-en-8-ium acetate ([DBU][Ac]) as a catalyst under ultrasound irradiation is described. Compared with other methods, this new method has the advantages of easier work-up, milder reaction conditions, high yields and environmentally benign procedure.
publishDate 2012
dc.date.none.fl_str_mv 2012-10-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012001000026
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012001000026
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532012005000051
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.23 n.10 2012
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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