New Adducts of Lapachol with Primary Amines
Autor(a) principal: | |
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Data de Publicação: | 2011 |
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=S0103-50532011000400025 |
Resumo: | New adducts of lapachol with neat primary aliphatic amines were obtained in a solvent-free reaction in good to reasonable yields (52 to 88%), at room temperature. The new compounds containing a phenazine moiety were obtained from suitable functionalized aminoalkyl compounds, including ethanolamine, 3-propanolamine, 2-methoxy-ethylamine, 3-methoxy-propylamine, n-butylamine and 2-phenetylamine. |
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Journal of the Brazilian Chemical Society (Online) |
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New Adducts of Lapachol with Primary Aminesphenazineslapacholnitrogen adductsquinones1,4-naphthoquinoneNew adducts of lapachol with neat primary aliphatic amines were obtained in a solvent-free reaction in good to reasonable yields (52 to 88%), at room temperature. The new compounds containing a phenazine moiety were obtained from suitable functionalized aminoalkyl compounds, including ethanolamine, 3-propanolamine, 2-methoxy-ethylamine, 3-methoxy-propylamine, n-butylamine and 2-phenetylamine.Sociedade Brasileira de Química2011-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000400025Journal of the Brazilian Chemical Society v.22 n.4 2011reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532011000400025info:eu-repo/semantics/openAccessSantos,Mirelly D. F.Litivack-Junior,José T.Antunes,Roberto V.Silva,Tania M. S.Camara,Celso A.eng2011-04-14T00:00:00Zoai:scielo:S0103-50532011000400025Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2011-04-14T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
New Adducts of Lapachol with Primary Amines |
title |
New Adducts of Lapachol with Primary Amines |
spellingShingle |
New Adducts of Lapachol with Primary Amines Santos,Mirelly D. F. phenazines lapachol nitrogen adducts quinones 1,4-naphthoquinone |
title_short |
New Adducts of Lapachol with Primary Amines |
title_full |
New Adducts of Lapachol with Primary Amines |
title_fullStr |
New Adducts of Lapachol with Primary Amines |
title_full_unstemmed |
New Adducts of Lapachol with Primary Amines |
title_sort |
New Adducts of Lapachol with Primary Amines |
author |
Santos,Mirelly D. F. |
author_facet |
Santos,Mirelly D. F. Litivack-Junior,José T. Antunes,Roberto V. Silva,Tania M. S. Camara,Celso A. |
author_role |
author |
author2 |
Litivack-Junior,José T. Antunes,Roberto V. Silva,Tania M. S. Camara,Celso A. |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Santos,Mirelly D. F. Litivack-Junior,José T. Antunes,Roberto V. Silva,Tania M. S. Camara,Celso A. |
dc.subject.por.fl_str_mv |
phenazines lapachol nitrogen adducts quinones 1,4-naphthoquinone |
topic |
phenazines lapachol nitrogen adducts quinones 1,4-naphthoquinone |
description |
New adducts of lapachol with neat primary aliphatic amines were obtained in a solvent-free reaction in good to reasonable yields (52 to 88%), at room temperature. The new compounds containing a phenazine moiety were obtained from suitable functionalized aminoalkyl compounds, including ethanolamine, 3-propanolamine, 2-methoxy-ethylamine, 3-methoxy-propylamine, n-butylamine and 2-phenetylamine. |
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=S0103-50532011000400025 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000400025 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-50532011000400025 |
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.22 n.4 2011 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_ |
1750318171985805312 |