NMR studies on 1,3-dipolar cycloaddition of nitrile oxides to norbornenes
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=S0103-50532013000500013 |
Resumo: | The 1,3-dipolar cycloaddition reaction of nitrile oxides to norbornenes substituted with an acrylate-derived moiety was examined. Only adducts to norbornene system were formed with a good exo selectivity and complete site-selectivity. Structures of the products were elucidated by an extensive application of electrospray ionization-mass spectrometry (ESI-MS) and 2D ¹H and 13C nuclear magnetic resonance (NMR). |
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NMR studies on 1,3-dipolar cycloaddition of nitrile oxides to norbornenes1,3-dipolar cycloadditionnorbornenesnitrile oxides2D NMRThe 1,3-dipolar cycloaddition reaction of nitrile oxides to norbornenes substituted with an acrylate-derived moiety was examined. Only adducts to norbornene system were formed with a good exo selectivity and complete site-selectivity. Structures of the products were elucidated by an extensive application of electrospray ionization-mass spectrometry (ESI-MS) and 2D ¹H and 13C nuclear magnetic resonance (NMR).Sociedade Brasileira de Química2013-05-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532013000500013Journal of the Brazilian Chemical Society v.24 n.5 2013reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.5935/0103-5053.20130106info:eu-repo/semantics/openAccessGucma,MirosławGołębiewski,W. MarekKrawczyk,Mariaeng2013-06-13T00:00:00Zoai:scielo:S0103-50532013000500013Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2013-06-13T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
NMR studies on 1,3-dipolar cycloaddition of nitrile oxides to norbornenes |
title |
NMR studies on 1,3-dipolar cycloaddition of nitrile oxides to norbornenes |
spellingShingle |
NMR studies on 1,3-dipolar cycloaddition of nitrile oxides to norbornenes Gucma,Mirosław 1,3-dipolar cycloaddition norbornenes nitrile oxides 2D NMR |
title_short |
NMR studies on 1,3-dipolar cycloaddition of nitrile oxides to norbornenes |
title_full |
NMR studies on 1,3-dipolar cycloaddition of nitrile oxides to norbornenes |
title_fullStr |
NMR studies on 1,3-dipolar cycloaddition of nitrile oxides to norbornenes |
title_full_unstemmed |
NMR studies on 1,3-dipolar cycloaddition of nitrile oxides to norbornenes |
title_sort |
NMR studies on 1,3-dipolar cycloaddition of nitrile oxides to norbornenes |
author |
Gucma,Mirosław |
author_facet |
Gucma,Mirosław Gołębiewski,W. Marek Krawczyk,Maria |
author_role |
author |
author2 |
Gołębiewski,W. Marek Krawczyk,Maria |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Gucma,Mirosław Gołębiewski,W. Marek Krawczyk,Maria |
dc.subject.por.fl_str_mv |
1,3-dipolar cycloaddition norbornenes nitrile oxides 2D NMR |
topic |
1,3-dipolar cycloaddition norbornenes nitrile oxides 2D NMR |
description |
The 1,3-dipolar cycloaddition reaction of nitrile oxides to norbornenes substituted with an acrylate-derived moiety was examined. Only adducts to norbornene system were formed with a good exo selectivity and complete site-selectivity. Structures of the products were elucidated by an extensive application of electrospray ionization-mass spectrometry (ESI-MS) and 2D ¹H and 13C nuclear magnetic resonance (NMR). |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-05-01 |
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=S0103-50532013000500013 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532013000500013 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.5935/0103-5053.20130106 |
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.5 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 |
_version_ |
1750318174859952128 |