Synthesis of Diiodo-Functionalized Benzo[b]furans via Electrophilic Iodocyclization

Detalhes bibliográficos
Autor(a) principal: Frota,Carlise
Data de Publicação: 2017
Outros Autores: Rossini,Allan F. C., Casagrande,Gleison A., Pizzuti,Lucas, Raminelli,Cristiano
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=S0103-50532017001002038
Resumo: An electrophilic iodocyclization reaction involving alkynylated 2-iodoanisoles and molecular iodine in the presence of sodium bicarbonate was developed and diiodo-functionalized benzo[b]furans were obtained in yields from 45 to 99%.
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spelling Synthesis of Diiodo-Functionalized Benzo[b]furans via Electrophilic Iodocyclizationelectrophilic iodocyclizationmolecular iodinediiodo-functionalized benzo[b]furansfunctionalized heteroaromaticsdiiodinated compoundsAn electrophilic iodocyclization reaction involving alkynylated 2-iodoanisoles and molecular iodine in the presence of sodium bicarbonate was developed and diiodo-functionalized benzo[b]furans were obtained in yields from 45 to 99%.Sociedade Brasileira de Química2017-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532017001002038Journal of the Brazilian Chemical Society v.28 n.10 2017reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0103-5053.20170035info:eu-repo/semantics/openAccessFrota,CarliseRossini,Allan F. C.Casagrande,Gleison A.Pizzuti,LucasRaminelli,Cristianoeng2017-09-22T00:00:00Zoai:scielo:S0103-50532017001002038Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2017-09-22T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Synthesis of Diiodo-Functionalized Benzo[b]furans via Electrophilic Iodocyclization
title Synthesis of Diiodo-Functionalized Benzo[b]furans via Electrophilic Iodocyclization
spellingShingle Synthesis of Diiodo-Functionalized Benzo[b]furans via Electrophilic Iodocyclization
Frota,Carlise
electrophilic iodocyclization
molecular iodine
diiodo-functionalized benzo[b]furans
functionalized heteroaromatics
diiodinated compounds
title_short Synthesis of Diiodo-Functionalized Benzo[b]furans via Electrophilic Iodocyclization
title_full Synthesis of Diiodo-Functionalized Benzo[b]furans via Electrophilic Iodocyclization
title_fullStr Synthesis of Diiodo-Functionalized Benzo[b]furans via Electrophilic Iodocyclization
title_full_unstemmed Synthesis of Diiodo-Functionalized Benzo[b]furans via Electrophilic Iodocyclization
title_sort Synthesis of Diiodo-Functionalized Benzo[b]furans via Electrophilic Iodocyclization
author Frota,Carlise
author_facet Frota,Carlise
Rossini,Allan F. C.
Casagrande,Gleison A.
Pizzuti,Lucas
Raminelli,Cristiano
author_role author
author2 Rossini,Allan F. C.
Casagrande,Gleison A.
Pizzuti,Lucas
Raminelli,Cristiano
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Frota,Carlise
Rossini,Allan F. C.
Casagrande,Gleison A.
Pizzuti,Lucas
Raminelli,Cristiano
dc.subject.por.fl_str_mv electrophilic iodocyclization
molecular iodine
diiodo-functionalized benzo[b]furans
functionalized heteroaromatics
diiodinated compounds
topic electrophilic iodocyclization
molecular iodine
diiodo-functionalized benzo[b]furans
functionalized heteroaromatics
diiodinated compounds
description An electrophilic iodocyclization reaction involving alkynylated 2-iodoanisoles and molecular iodine in the presence of sodium bicarbonate was developed and diiodo-functionalized benzo[b]furans were obtained in yields from 45 to 99%.
publishDate 2017
dc.date.none.fl_str_mv 2017-10-01
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=S0103-50532017001002038
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532017001002038
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.21577/0103-5053.20170035
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.28 n.10 2017
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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