Studies towards the identification of the sex pheromone of Thyrinteina arnobia
Autor(a) principal: | |
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Data de Publicação: | 2013 |
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=S0103-50532013001200006 |
Resumo: | The eucalyptus brown-looper Thyrinteina arnobia (Lepidoptera: Geometridae) is considered an important pest in Brazilian native plants, e.g. Psidium guajava, and exotic plants, such as Eucalyptus species. In this work we describe the isolation of the pheromone components of T. arnobia, using glands extract and solid phase micro extraction (SPME) of virgin females. The samples were analyzed by gas chromatography with an electroantennographic detector (GC-EAD), and mass spectrometry (GC-MS). Two reproducible electroantennographic responses were elicited in the male antenna of T. arnobia and one of them was identified as 3,4-epoxy-6,9-heneicosadiene by CG-MS. The racemic synthesis of this epoxydiene was carried out in 10 steps and 28% overall yield. The four stereoisomers of the epoxydiene were also synthesized employing the corresponding enantiomeric enriched epoxyalcohols. |
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Studies towards the identification of the sex pheromone of Thyrinteina arnobiaelectroantennographyThyrinteina arnobiasex pheromone3,4-epoxy-Z6,Z9-heneicosadieneasymmetric synthesisThe eucalyptus brown-looper Thyrinteina arnobia (Lepidoptera: Geometridae) is considered an important pest in Brazilian native plants, e.g. Psidium guajava, and exotic plants, such as Eucalyptus species. In this work we describe the isolation of the pheromone components of T. arnobia, using glands extract and solid phase micro extraction (SPME) of virgin females. The samples were analyzed by gas chromatography with an electroantennographic detector (GC-EAD), and mass spectrometry (GC-MS). Two reproducible electroantennographic responses were elicited in the male antenna of T. arnobia and one of them was identified as 3,4-epoxy-6,9-heneicosadiene by CG-MS. The racemic synthesis of this epoxydiene was carried out in 10 steps and 28% overall yield. The four stereoisomers of the epoxydiene were also synthesized employing the corresponding enantiomeric enriched epoxyalcohols.Sociedade Brasileira de Química2013-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532013001200006Journal of the Brazilian Chemical Society v.24 n.12 2013reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.5935/0103-5053.20130241info:eu-repo/semantics/openAccessMoreira,Jardel A.Neppe,TiagoPaiva,Marcelo M. deDeobald,Anna M.Batista-Pereira,Luciane G.Paixão,Marcio W.Corrêa,Arlene G.eng2013-12-09T00:00:00Zoai:scielo:S0103-50532013001200006Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2013-12-09T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Studies towards the identification of the sex pheromone of Thyrinteina arnobia |
title |
Studies towards the identification of the sex pheromone of Thyrinteina arnobia |
spellingShingle |
Studies towards the identification of the sex pheromone of Thyrinteina arnobia Moreira,Jardel A. electroantennography Thyrinteina arnobia sex pheromone 3,4-epoxy-Z6,Z9-heneicosadiene asymmetric synthesis |
title_short |
Studies towards the identification of the sex pheromone of Thyrinteina arnobia |
title_full |
Studies towards the identification of the sex pheromone of Thyrinteina arnobia |
title_fullStr |
Studies towards the identification of the sex pheromone of Thyrinteina arnobia |
title_full_unstemmed |
Studies towards the identification of the sex pheromone of Thyrinteina arnobia |
title_sort |
Studies towards the identification of the sex pheromone of Thyrinteina arnobia |
author |
Moreira,Jardel A. |
author_facet |
Moreira,Jardel A. Neppe,Tiago Paiva,Marcelo M. de Deobald,Anna M. Batista-Pereira,Luciane G. Paixão,Marcio W. Corrêa,Arlene G. |
author_role |
author |
author2 |
Neppe,Tiago Paiva,Marcelo M. de Deobald,Anna M. Batista-Pereira,Luciane G. Paixão,Marcio W. Corrêa,Arlene G. |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Moreira,Jardel A. Neppe,Tiago Paiva,Marcelo M. de Deobald,Anna M. Batista-Pereira,Luciane G. Paixão,Marcio W. Corrêa,Arlene G. |
dc.subject.por.fl_str_mv |
electroantennography Thyrinteina arnobia sex pheromone 3,4-epoxy-Z6,Z9-heneicosadiene asymmetric synthesis |
topic |
electroantennography Thyrinteina arnobia sex pheromone 3,4-epoxy-Z6,Z9-heneicosadiene asymmetric synthesis |
description |
The eucalyptus brown-looper Thyrinteina arnobia (Lepidoptera: Geometridae) is considered an important pest in Brazilian native plants, e.g. Psidium guajava, and exotic plants, such as Eucalyptus species. In this work we describe the isolation of the pheromone components of T. arnobia, using glands extract and solid phase micro extraction (SPME) of virgin females. The samples were analyzed by gas chromatography with an electroantennographic detector (GC-EAD), and mass spectrometry (GC-MS). Two reproducible electroantennographic responses were elicited in the male antenna of T. arnobia and one of them was identified as 3,4-epoxy-6,9-heneicosadiene by CG-MS. The racemic synthesis of this epoxydiene was carried out in 10 steps and 28% overall yield. The four stereoisomers of the epoxydiene were also synthesized employing the corresponding enantiomeric enriched epoxyalcohols. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-12-01 |
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=S0103-50532013001200006 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532013001200006 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.5935/0103-5053.20130241 |
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.24 n.12 2013 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 |
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1750318175348588544 |