Anodic methoxylation of cinnamate esters

Detalhes bibliográficos
Autor(a) principal: Pardini,Vera L.
Data de Publicação: 2001
Outros Autores: Sakata,Solange K., Vargas,Reinaldo R., Viertler,Hans
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=S0103-50532001000200016
Resumo: The present work describes the electrochemical oxidation of methyl cinnamate ring methoxylated derivatives in neutral or basic methanolic solution. In the electrochemical studies cyclic voltammetry and preparative electrolyses under controlled potential or current conditions in divided or undivided cells were used. The influence of current density, cell type, electrode material, solvent, substrate and base concentration was investigated for methyl 4-methoxycinnamate.The products result from aromatic ring and side chain methoxylation, however, nuclear methoxylation products were observed in higher yields when the number of methoxy groups in the aromatic ring was increased. The structure of the products is dependent on the work-up procedures.
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spelling Anodic methoxylation of cinnamate esterselectrochemical oxidationanodic methoxylationmethyl cinnamate derivativesThe present work describes the electrochemical oxidation of methyl cinnamate ring methoxylated derivatives in neutral or basic methanolic solution. In the electrochemical studies cyclic voltammetry and preparative electrolyses under controlled potential or current conditions in divided or undivided cells were used. The influence of current density, cell type, electrode material, solvent, substrate and base concentration was investigated for methyl 4-methoxycinnamate.The products result from aromatic ring and side chain methoxylation, however, nuclear methoxylation products were observed in higher yields when the number of methoxy groups in the aromatic ring was increased. The structure of the products is dependent on the work-up procedures.Sociedade Brasileira de Química2001-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532001000200016Journal of the Brazilian Chemical Society v.12 n.2 2001reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532001000200016info:eu-repo/semantics/openAccessPardini,Vera L.Sakata,Solange K.Vargas,Reinaldo R.Viertler,Hanseng2001-07-02T00:00:00Zoai:scielo:S0103-50532001000200016Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2001-07-02T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Anodic methoxylation of cinnamate esters
title Anodic methoxylation of cinnamate esters
spellingShingle Anodic methoxylation of cinnamate esters
Pardini,Vera L.
electrochemical oxidation
anodic methoxylation
methyl cinnamate derivatives
title_short Anodic methoxylation of cinnamate esters
title_full Anodic methoxylation of cinnamate esters
title_fullStr Anodic methoxylation of cinnamate esters
title_full_unstemmed Anodic methoxylation of cinnamate esters
title_sort Anodic methoxylation of cinnamate esters
author Pardini,Vera L.
author_facet Pardini,Vera L.
Sakata,Solange K.
Vargas,Reinaldo R.
Viertler,Hans
author_role author
author2 Sakata,Solange K.
Vargas,Reinaldo R.
Viertler,Hans
author2_role author
author
author
dc.contributor.author.fl_str_mv Pardini,Vera L.
Sakata,Solange K.
Vargas,Reinaldo R.
Viertler,Hans
dc.subject.por.fl_str_mv electrochemical oxidation
anodic methoxylation
methyl cinnamate derivatives
topic electrochemical oxidation
anodic methoxylation
methyl cinnamate derivatives
description The present work describes the electrochemical oxidation of methyl cinnamate ring methoxylated derivatives in neutral or basic methanolic solution. In the electrochemical studies cyclic voltammetry and preparative electrolyses under controlled potential or current conditions in divided or undivided cells were used. The influence of current density, cell type, electrode material, solvent, substrate and base concentration was investigated for methyl 4-methoxycinnamate.The products result from aromatic ring and side chain methoxylation, however, nuclear methoxylation products were observed in higher yields when the number of methoxy groups in the aromatic ring was increased. The structure of the products is dependent on the work-up procedures.
publishDate 2001
dc.date.none.fl_str_mv 2001-04-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532001000200016
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532001000200016
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532001000200016
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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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.12 n.2 2001
reponame:Journal of the Brazilian Chemical Society (Online)
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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
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