A general and efficient synthesis of pyrazoles catalyzed by Sc(OTf)3 under solvent-free conditions

Detalhes bibliográficos
Autor(a) principal: Xiong,Wei
Data de Publicação: 2009
Outros Autores: Chen,Jiu-Xi, Liu,Miao-Chang, Ding,Jin-Chang, Wu,Hua-Yue, Su,Wei-Ke
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=S0103-50532009000200023
Resumo: Pyrazoles were prepared in excellent yields via solventless condensation of various 1,3-diketones (R¹COCHXCOCH3, R¹ = Me, Ph; X = H, Me, Cl) and hydrazines, acylhydrazines or sulfonyl hydrazines in the presence of a catalytic amount of Sc(OTf)3 at room temperature. Additionally, the catalyst could be recovered easily after the reactions and reused without evident loss in activity.
id SBQ-2_6aab1fca8d5423adf8097fe1a46959cf
oai_identifier_str oai:scielo:S0103-50532009000200023
network_acronym_str SBQ-2
network_name_str Journal of the Brazilian Chemical Society (Online)
repository_id_str
spelling A general and efficient synthesis of pyrazoles catalyzed by Sc(OTf)3 under solvent-free conditionsscandium(III) triflatepyrazoles1,3-diketoneshydrazineshydrazidessolvent-freePyrazoles were prepared in excellent yields via solventless condensation of various 1,3-diketones (R¹COCHXCOCH3, R¹ = Me, Ph; X = H, Me, Cl) and hydrazines, acylhydrazines or sulfonyl hydrazines in the presence of a catalytic amount of Sc(OTf)3 at room temperature. Additionally, the catalyst could be recovered easily after the reactions and reused without evident loss in activity.Sociedade Brasileira de Química2009-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000200023Journal of the Brazilian Chemical Society v.20 n.2 2009reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532009000200023info:eu-repo/semantics/openAccessXiong,WeiChen,Jiu-XiLiu,Miao-ChangDing,Jin-ChangWu,Hua-YueSu,Wei-Keeng2009-02-27T00:00:00Zoai:scielo:S0103-50532009000200023Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2009-02-27T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv A general and efficient synthesis of pyrazoles catalyzed by Sc(OTf)3 under solvent-free conditions
title A general and efficient synthesis of pyrazoles catalyzed by Sc(OTf)3 under solvent-free conditions
spellingShingle A general and efficient synthesis of pyrazoles catalyzed by Sc(OTf)3 under solvent-free conditions
Xiong,Wei
scandium(III) triflate
pyrazoles
1,3-diketones
hydrazines
hydrazides
solvent-free
title_short A general and efficient synthesis of pyrazoles catalyzed by Sc(OTf)3 under solvent-free conditions
title_full A general and efficient synthesis of pyrazoles catalyzed by Sc(OTf)3 under solvent-free conditions
title_fullStr A general and efficient synthesis of pyrazoles catalyzed by Sc(OTf)3 under solvent-free conditions
title_full_unstemmed A general and efficient synthesis of pyrazoles catalyzed by Sc(OTf)3 under solvent-free conditions
title_sort A general and efficient synthesis of pyrazoles catalyzed by Sc(OTf)3 under solvent-free conditions
author Xiong,Wei
author_facet Xiong,Wei
Chen,Jiu-Xi
Liu,Miao-Chang
Ding,Jin-Chang
Wu,Hua-Yue
Su,Wei-Ke
author_role author
author2 Chen,Jiu-Xi
Liu,Miao-Chang
Ding,Jin-Chang
Wu,Hua-Yue
Su,Wei-Ke
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Xiong,Wei
Chen,Jiu-Xi
Liu,Miao-Chang
Ding,Jin-Chang
Wu,Hua-Yue
Su,Wei-Ke
dc.subject.por.fl_str_mv scandium(III) triflate
pyrazoles
1,3-diketones
hydrazines
hydrazides
solvent-free
topic scandium(III) triflate
pyrazoles
1,3-diketones
hydrazines
hydrazides
solvent-free
description Pyrazoles were prepared in excellent yields via solventless condensation of various 1,3-diketones (R¹COCHXCOCH3, R¹ = Me, Ph; X = H, Me, Cl) and hydrazines, acylhydrazines or sulfonyl hydrazines in the presence of a catalytic amount of Sc(OTf)3 at room temperature. Additionally, the catalyst could be recovered easily after the reactions and reused without evident loss in activity.
publishDate 2009
dc.date.none.fl_str_mv 2009-01-01
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=S0103-50532009000200023
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000200023
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532009000200023
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.20 n.2 2009
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
_version_ 1750318169764921344