Métodos sintéticos para preparação de 2,2'-bipiridinas substituídas
The 2,2'-bipyridine has been entitled as the most widely used ligand. Nowadays there is a large variety of known molecules comprising at least two 2,2'-bipyridine units and the number of applications in many areas such as catalysis, new materials, optoeletronics and electrochemistry have i...
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Sociedade Brasileira de Química
2002-01-01
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doaj-1be2b09ed3dc45e9a30c7907f74cfe562020-11-24T23:32:20ZengSociedade Brasileira de QuímicaQuímica Nova0100-40421678-70642002-01-01254668675Métodos sintéticos para preparação de 2,2'-bipiridinas substituídasDonnici Claudio LuisOliveira Ione Maria Ferreira deTemba Eliane Sílvia CodoCastro Maurício Costa Rogério deThe 2,2'-bipyridine has been entitled as the most widely used ligand. Nowadays there is a large variety of known molecules comprising at least two 2,2'-bipyridine units and the number of applications in many areas such as catalysis, new materials, optoeletronics and electrochemistry have increased very much in the past decades. Nevertheless, there is no article that gives an overview of the main synthetic methods for obtaining the substituted 2,2'-bipyridines, generally non available. This article presents a synthetic discussion about the three different methods (coupling reaction, ciclo-functionalization and functionalization of the heteroaromatic rings of 2,2'-bipyridine) for preparing these heterocyclic compounds and also provides a practical and fundamental guide, for obtaining more than eighty different symmetric and unsymmetrical substituted 2,2'-bipyridines, shown in a table with the corresponding references.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-404220020004000232,2'-bipyridinessynthesiscouplingfunctionalization |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Donnici Claudio Luis Oliveira Ione Maria Ferreira de Temba Eliane Sílvia Codo Castro Maurício Costa Rogério de |
spellingShingle |
Donnici Claudio Luis Oliveira Ione Maria Ferreira de Temba Eliane Sílvia Codo Castro Maurício Costa Rogério de Métodos sintéticos para preparação de 2,2'-bipiridinas substituídas Química Nova 2,2'-bipyridines synthesis coupling functionalization |
author_facet |
Donnici Claudio Luis Oliveira Ione Maria Ferreira de Temba Eliane Sílvia Codo Castro Maurício Costa Rogério de |
author_sort |
Donnici Claudio Luis |
title |
Métodos sintéticos para preparação de 2,2'-bipiridinas substituídas |
title_short |
Métodos sintéticos para preparação de 2,2'-bipiridinas substituídas |
title_full |
Métodos sintéticos para preparação de 2,2'-bipiridinas substituídas |
title_fullStr |
Métodos sintéticos para preparação de 2,2'-bipiridinas substituídas |
title_full_unstemmed |
Métodos sintéticos para preparação de 2,2'-bipiridinas substituídas |
title_sort |
métodos sintéticos para preparação de 2,2'-bipiridinas substituídas |
publisher |
Sociedade Brasileira de Química |
series |
Química Nova |
issn |
0100-4042 1678-7064 |
publishDate |
2002-01-01 |
description |
The 2,2'-bipyridine has been entitled as the most widely used ligand. Nowadays there is a large variety of known molecules comprising at least two 2,2'-bipyridine units and the number of applications in many areas such as catalysis, new materials, optoeletronics and electrochemistry have increased very much in the past decades. Nevertheless, there is no article that gives an overview of the main synthetic methods for obtaining the substituted 2,2'-bipyridines, generally non available. This article presents a synthetic discussion about the three different methods (coupling reaction, ciclo-functionalization and functionalization of the heteroaromatic rings of 2,2'-bipyridine) for preparing these heterocyclic compounds and also provides a practical and fundamental guide, for obtaining more than eighty different symmetric and unsymmetrical substituted 2,2'-bipyridines, shown in a table with the corresponding references. |
topic |
2,2'-bipyridines synthesis coupling functionalization |
url |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422002000400023 |
work_keys_str_mv |
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