An easy synthesis of 3,5-disubstituted 1,2,4-oxadiazoles from carboxylic acids and arylamidoximes mediated by ethyl chloroformate
| Autor(a) principal: | |
|---|---|
| Data de Publicação: | 2009 |
| Outros Autores: | , , |
| 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=S0103-50532009000700023 |
Resumo: | An efficient, clean and easy high-yielding synthesis of 3,5-disubstituted 1,2,4-oxadiazoles starting from mixed anhydrides (generated from carboxylic acids and ethyl chloroformate) and arylamidoximes is described. |
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An easy synthesis of 3,5-disubstituted 1,2,4-oxadiazoles from carboxylic acids and arylamidoximes mediated by ethyl chloroformatecarboxylic acidsarylamidoximes1,2,4-oxadiazoles1H and 13C NMR spectraAn efficient, clean and easy high-yielding synthesis of 3,5-disubstituted 1,2,4-oxadiazoles starting from mixed anhydrides (generated from carboxylic acids and ethyl chloroformate) and arylamidoximes is described.Sociedade Brasileira de Química2009-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000700023Journal of the Brazilian Chemical Society v.20 n.7 2009reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532009000700023info:eu-repo/semantics/openAccessNeves Filho,Ricardo A. W.Bezerra,Natércia M. M.Guedes,José M.Srivastava,Rajendra M.eng2009-08-28T00:00:00Zoai:scielo:S0103-50532009000700023Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2009-08-28T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
| dc.title.none.fl_str_mv |
An easy synthesis of 3,5-disubstituted 1,2,4-oxadiazoles from carboxylic acids and arylamidoximes mediated by ethyl chloroformate |
| title |
An easy synthesis of 3,5-disubstituted 1,2,4-oxadiazoles from carboxylic acids and arylamidoximes mediated by ethyl chloroformate |
| spellingShingle |
An easy synthesis of 3,5-disubstituted 1,2,4-oxadiazoles from carboxylic acids and arylamidoximes mediated by ethyl chloroformate Neves Filho,Ricardo A. W. carboxylic acids arylamidoximes 1,2,4-oxadiazoles 1H and 13C NMR spectra |
| title_short |
An easy synthesis of 3,5-disubstituted 1,2,4-oxadiazoles from carboxylic acids and arylamidoximes mediated by ethyl chloroformate |
| title_full |
An easy synthesis of 3,5-disubstituted 1,2,4-oxadiazoles from carboxylic acids and arylamidoximes mediated by ethyl chloroformate |
| title_fullStr |
An easy synthesis of 3,5-disubstituted 1,2,4-oxadiazoles from carboxylic acids and arylamidoximes mediated by ethyl chloroformate |
| title_full_unstemmed |
An easy synthesis of 3,5-disubstituted 1,2,4-oxadiazoles from carboxylic acids and arylamidoximes mediated by ethyl chloroformate |
| title_sort |
An easy synthesis of 3,5-disubstituted 1,2,4-oxadiazoles from carboxylic acids and arylamidoximes mediated by ethyl chloroformate |
| author |
Neves Filho,Ricardo A. W. |
| author_facet |
Neves Filho,Ricardo A. W. Bezerra,Natércia M. M. Guedes,José M. Srivastava,Rajendra M. |
| author_role |
author |
| author2 |
Bezerra,Natércia M. M. Guedes,José M. Srivastava,Rajendra M. |
| author2_role |
author author author |
| dc.contributor.author.fl_str_mv |
Neves Filho,Ricardo A. W. Bezerra,Natércia M. M. Guedes,José M. Srivastava,Rajendra M. |
| dc.subject.por.fl_str_mv |
carboxylic acids arylamidoximes 1,2,4-oxadiazoles 1H and 13C NMR spectra |
| topic |
carboxylic acids arylamidoximes 1,2,4-oxadiazoles 1H and 13C NMR spectra |
| description |
An efficient, clean and easy high-yielding synthesis of 3,5-disubstituted 1,2,4-oxadiazoles starting from mixed anhydrides (generated from carboxylic acids and ethyl chloroformate) and arylamidoximes is described. |
| 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 |
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publishedVersion |
| dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000700023 |
| url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000700023 |
| dc.language.iso.fl_str_mv |
eng |
| language |
eng |
| dc.relation.none.fl_str_mv |
10.1590/S0103-50532009000700023 |
| 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.7 2009 reponame:Journal of the Brazilian Chemical Society (Online) instname:Sociedade Brasileira de Química (SBQ) instacron:SBQ |
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Sociedade Brasileira de Química (SBQ) |
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SBQ |
| institution |
SBQ |
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Journal of the Brazilian Chemical Society (Online) |
| collection |
Journal of the Brazilian Chemical Society (Online) |
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Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ) |
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||office@jbcs.sbq.org.br |
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1750318170210566144 |