Al(HSO4)3 as an efficient catalyst for acetalization of carbonyl compounds under heterogeneous or solvent -free conditions

Detalhes bibliográficos
Autor(a) principal: Mirjalili,BiBi Fatemeh
Data de Publicação: 2005
Outros Autores: Zolfigol,Mohammad Ali, Bamoniri,Abdolhamid, Hazar,Azizeh
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=S0103-50532005000500031
Resumo: Al(HSO4)3 as a solid acid was applied for acetalization of carbonyl compounds at room temperature and under solvent-free conditions with good to excellent yields. The cheapness and availability of this reagent with easy procedure and work-up make this method attractive for the organic synthesis.
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spelling Al(HSO4)3 as an efficient catalyst for acetalization of carbonyl compounds under heterogeneous or solvent -free conditionsacetalizationsolvent-freesolid acidAl(HSO4)3carbonyl compoundheterogeneous conditionAl(HSO4)3 as a solid acid was applied for acetalization of carbonyl compounds at room temperature and under solvent-free conditions with good to excellent yields. The cheapness and availability of this reagent with easy procedure and work-up make this method attractive for the organic synthesis.Sociedade Brasileira de Química2005-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532005000500031Journal of the Brazilian Chemical Society v.16 n.4 2005reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532005000500031info:eu-repo/semantics/openAccessMirjalili,BiBi FatemehZolfigol,Mohammad AliBamoniri,AbdolhamidHazar,Azizeheng2005-08-25T00:00:00Zoai:scielo:S0103-50532005000500031Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2005-08-25T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Al(HSO4)3 as an efficient catalyst for acetalization of carbonyl compounds under heterogeneous or solvent -free conditions
title Al(HSO4)3 as an efficient catalyst for acetalization of carbonyl compounds under heterogeneous or solvent -free conditions
spellingShingle Al(HSO4)3 as an efficient catalyst for acetalization of carbonyl compounds under heterogeneous or solvent -free conditions
Mirjalili,BiBi Fatemeh
acetalization
solvent-free
solid acid
Al(HSO4)3
carbonyl compound
heterogeneous condition
title_short Al(HSO4)3 as an efficient catalyst for acetalization of carbonyl compounds under heterogeneous or solvent -free conditions
title_full Al(HSO4)3 as an efficient catalyst for acetalization of carbonyl compounds under heterogeneous or solvent -free conditions
title_fullStr Al(HSO4)3 as an efficient catalyst for acetalization of carbonyl compounds under heterogeneous or solvent -free conditions
title_full_unstemmed Al(HSO4)3 as an efficient catalyst for acetalization of carbonyl compounds under heterogeneous or solvent -free conditions
title_sort Al(HSO4)3 as an efficient catalyst for acetalization of carbonyl compounds under heterogeneous or solvent -free conditions
author Mirjalili,BiBi Fatemeh
author_facet Mirjalili,BiBi Fatemeh
Zolfigol,Mohammad Ali
Bamoniri,Abdolhamid
Hazar,Azizeh
author_role author
author2 Zolfigol,Mohammad Ali
Bamoniri,Abdolhamid
Hazar,Azizeh
author2_role author
author
author
dc.contributor.author.fl_str_mv Mirjalili,BiBi Fatemeh
Zolfigol,Mohammad Ali
Bamoniri,Abdolhamid
Hazar,Azizeh
dc.subject.por.fl_str_mv acetalization
solvent-free
solid acid
Al(HSO4)3
carbonyl compound
heterogeneous condition
topic acetalization
solvent-free
solid acid
Al(HSO4)3
carbonyl compound
heterogeneous condition
description Al(HSO4)3 as a solid acid was applied for acetalization of carbonyl compounds at room temperature and under solvent-free conditions with good to excellent yields. The cheapness and availability of this reagent with easy procedure and work-up make this method attractive for the organic synthesis.
publishDate 2005
dc.date.none.fl_str_mv 2005-08-01
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=S0103-50532005000500031
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532005000500031
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532005000500031
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.16 n.4 2005
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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