A reação "click" na síntese de 1,2,3-triazóis: aspectos químicos e aplicações
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Química Nova (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422011001000012 |
Resumo: | The Copper-catalyzed azide-alkyne cycloaddition (CuAAC), often referred to as "click" reaction, has become a very popular reaction in the last years. It affords exclusively 1,4-disubstituted 1,2,3-triazoles and has been widely used to connect readily accessible building blocks containing various functional groups. The great success of this reaction is based on the fact that it is general, virtually quantitative and very robuste. The scope of this copper-catalyzed synthesis is extraordinary and the reaction has found numerous applications in many research fields, including biological chemistry and materials science. In this review, the main chemical aspects and applications of the "click" reaction in the synthesis of 1,2,3-triazoles are presented. |
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A reação "click" na síntese de 1,2,3-triazóis: aspectos químicos e aplicaçõesclickreactioncycloadditiontriazoleThe Copper-catalyzed azide-alkyne cycloaddition (CuAAC), often referred to as "click" reaction, has become a very popular reaction in the last years. It affords exclusively 1,4-disubstituted 1,2,3-triazoles and has been widely used to connect readily accessible building blocks containing various functional groups. The great success of this reaction is based on the fact that it is general, virtually quantitative and very robuste. The scope of this copper-catalyzed synthesis is extraordinary and the reaction has found numerous applications in many research fields, including biological chemistry and materials science. In this review, the main chemical aspects and applications of the "click" reaction in the synthesis of 1,2,3-triazoles are presented.Sociedade Brasileira de Química2011-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422011001000012Química Nova v.34 n.10 2011reponame:Química Nova (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0100-40422011001000012info:eu-repo/semantics/openAccessFreitas,Luiza Baptista de OliveiraRuela,Fernando ArminiPereira,Guilherme RochaAlves,Rosemeire BrondiFreitas,Rossimiriam Pereira deSantos,Leandro José dospor2011-12-06T00:00:00Zoai:scielo:S0100-40422011001000012Revistahttps://www.scielo.br/j/qn/ONGhttps://old.scielo.br/oai/scielo-oai.phpquimicanova@sbq.org.br1678-70640100-4042opendoar:2011-12-06T00:00Química Nova (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
A reação "click" na síntese de 1,2,3-triazóis: aspectos químicos e aplicações |
title |
A reação "click" na síntese de 1,2,3-triazóis: aspectos químicos e aplicações |
spellingShingle |
A reação "click" na síntese de 1,2,3-triazóis: aspectos químicos e aplicações Freitas,Luiza Baptista de Oliveira click reaction cycloaddition triazole |
title_short |
A reação "click" na síntese de 1,2,3-triazóis: aspectos químicos e aplicações |
title_full |
A reação "click" na síntese de 1,2,3-triazóis: aspectos químicos e aplicações |
title_fullStr |
A reação "click" na síntese de 1,2,3-triazóis: aspectos químicos e aplicações |
title_full_unstemmed |
A reação "click" na síntese de 1,2,3-triazóis: aspectos químicos e aplicações |
title_sort |
A reação "click" na síntese de 1,2,3-triazóis: aspectos químicos e aplicações |
author |
Freitas,Luiza Baptista de Oliveira |
author_facet |
Freitas,Luiza Baptista de Oliveira Ruela,Fernando Armini Pereira,Guilherme Rocha Alves,Rosemeire Brondi Freitas,Rossimiriam Pereira de Santos,Leandro José dos |
author_role |
author |
author2 |
Ruela,Fernando Armini Pereira,Guilherme Rocha Alves,Rosemeire Brondi Freitas,Rossimiriam Pereira de Santos,Leandro José dos |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Freitas,Luiza Baptista de Oliveira Ruela,Fernando Armini Pereira,Guilherme Rocha Alves,Rosemeire Brondi Freitas,Rossimiriam Pereira de Santos,Leandro José dos |
dc.subject.por.fl_str_mv |
click reaction cycloaddition triazole |
topic |
click reaction cycloaddition triazole |
description |
The Copper-catalyzed azide-alkyne cycloaddition (CuAAC), often referred to as "click" reaction, has become a very popular reaction in the last years. It affords exclusively 1,4-disubstituted 1,2,3-triazoles and has been widely used to connect readily accessible building blocks containing various functional groups. The great success of this reaction is based on the fact that it is general, virtually quantitative and very robuste. The scope of this copper-catalyzed synthesis is extraordinary and the reaction has found numerous applications in many research fields, including biological chemistry and materials science. In this review, the main chemical aspects and applications of the "click" reaction in the synthesis of 1,2,3-triazoles are presented. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-01-01 |
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=S0100-40422011001000012 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422011001000012 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
10.1590/S0100-40422011001000012 |
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 |
Química Nova v.34 n.10 2011 reponame:Química Nova (Online) instname:Sociedade Brasileira de Química (SBQ) instacron:SBQ |
instname_str |
Sociedade Brasileira de Química (SBQ) |
instacron_str |
SBQ |
institution |
SBQ |
reponame_str |
Química Nova (Online) |
collection |
Química Nova (Online) |
repository.name.fl_str_mv |
Química Nova (Online) - Sociedade Brasileira de Química (SBQ) |
repository.mail.fl_str_mv |
quimicanova@sbq.org.br |
_version_ |
1750318112731824128 |