Enantioselective synthesis of (R)-isocarvone from (S)-perillaldehyde

Detalhes bibliográficos
Autor(a) principal: Gamba,Douglas
Data de Publicação: 2008
Outros Autores: Pisoni,Diego S., Costa,Jessie S. da, Petzhold,Cesar L., Borges,Antonio C. A., Ceschi,Marco A.
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=S0103-50532008000700007
Resumo: This work describes the enantioselective preparation of (R)-(+)-isocarvone, (S)-(-)-5-isopropenylcyclohex-2-enone and (S)-(-)-3-isopropenylcyclohexanone starting from (S)-(-)-perillaldehyde. These compounds hold the prospect of serving as useful chiral building blocks or intermediates in organic synthesis.
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spelling Enantioselective synthesis of (R)-isocarvone from (S)-perillaldehydeisocarvonepreparationperillaldehydebuilding blockcyclohex-2-enoneThis work describes the enantioselective preparation of (R)-(+)-isocarvone, (S)-(-)-5-isopropenylcyclohex-2-enone and (S)-(-)-3-isopropenylcyclohexanone starting from (S)-(-)-perillaldehyde. These compounds hold the prospect of serving as useful chiral building blocks or intermediates in organic synthesis.Sociedade Brasileira de Química2008-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532008000700007Journal of the Brazilian Chemical Society v.19 n.7 2008reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532008000700007info:eu-repo/semantics/openAccessGamba,DouglasPisoni,Diego S.Costa,Jessie S. daPetzhold,Cesar L.Borges,Antonio C. A.Ceschi,Marco A.eng2017-05-05T00:00:00Zoai:scielo:S0103-50532008000700007Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2017-05-05T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Enantioselective synthesis of (R)-isocarvone from (S)-perillaldehyde
title Enantioselective synthesis of (R)-isocarvone from (S)-perillaldehyde
spellingShingle Enantioselective synthesis of (R)-isocarvone from (S)-perillaldehyde
Gamba,Douglas
isocarvone
preparation
perillaldehyde
building block
cyclohex-2-enone
title_short Enantioselective synthesis of (R)-isocarvone from (S)-perillaldehyde
title_full Enantioselective synthesis of (R)-isocarvone from (S)-perillaldehyde
title_fullStr Enantioselective synthesis of (R)-isocarvone from (S)-perillaldehyde
title_full_unstemmed Enantioselective synthesis of (R)-isocarvone from (S)-perillaldehyde
title_sort Enantioselective synthesis of (R)-isocarvone from (S)-perillaldehyde
author Gamba,Douglas
author_facet Gamba,Douglas
Pisoni,Diego S.
Costa,Jessie S. da
Petzhold,Cesar L.
Borges,Antonio C. A.
Ceschi,Marco A.
author_role author
author2 Pisoni,Diego S.
Costa,Jessie S. da
Petzhold,Cesar L.
Borges,Antonio C. A.
Ceschi,Marco A.
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Gamba,Douglas
Pisoni,Diego S.
Costa,Jessie S. da
Petzhold,Cesar L.
Borges,Antonio C. A.
Ceschi,Marco A.
dc.subject.por.fl_str_mv isocarvone
preparation
perillaldehyde
building block
cyclohex-2-enone
topic isocarvone
preparation
perillaldehyde
building block
cyclohex-2-enone
description This work describes the enantioselective preparation of (R)-(+)-isocarvone, (S)-(-)-5-isopropenylcyclohex-2-enone and (S)-(-)-3-isopropenylcyclohexanone starting from (S)-(-)-perillaldehyde. These compounds hold the prospect of serving as useful chiral building blocks or intermediates in organic synthesis.
publishDate 2008
dc.date.none.fl_str_mv 2008-01-01
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=S0103-50532008000700007
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532008000700007
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532008000700007
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.19 n.7 2008
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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