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. [UNIFESP], Casagrande, Gleison A., Pizzuti, Lucas, Raminelli, Cristiano [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: https://repositorio.unifesp.br/handle/11600/57314
http://dx.doi.org/10.21577/0103-5053.20170035
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 Frota, CarliseRossini, Allan F. C. [UNIFESP]Casagrande, Gleison A.Pizzuti, LucasRaminelli, Cristiano [UNIFESP]2020-08-04T13:40:08Z2020-08-04T13:40:08Z2017Journal Of The Brazilian Chemical Society. Sao Paulo, v. 28, n. 10, p. 2038-2044, 2017.0103-5053https://repositorio.unifesp.br/handle/11600/57314http://dx.doi.org/10.21577/0103-5053.20170035S0103-50532017001002038.pdfS0103-5053201700100203810.21577/0103-5053.20170035WOS:000411813200025An 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%.Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)Fundacao de Apoio ao Desenvolvimento do Ensino, Ciencia e Tecnologia do Estado de Mato Grosso do Sul (FUNDECT)Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)Fundacao Univ Fed Grande Dourados, Grp Pesquisa Sintese & Caracterizacao Mol MS, Rua Joao Rosa Goes,1761, BR-79825070 Dourados, MS, BrazilUniv Fed Sao Paulo, Inst Ciencias Ambientais Quim & Farmaceut, Rua Prof Artur Riedel,275, BR-09972270 Diadema, SP, BrazilUniv Fed Sao Paulo, Inst Ciencias Ambientais Quim & Farmaceut, Rua Prof Artur Riedel,275, BR-09972270 Diadema, SP, BrazilWeb of Science2038-2044engSoc Brasileira QuimicaJournal Of The Brazilian Chemical Societyelectrophilic iodocyclizationmolecular iodinediiodo-functionalized benzo[b] furansfunctionalized heteroaromaticsdiiodinated compoundsSynthesis of Diiodo-Functionalized Benzo[b] furans via Electrophilic Iodocyclizationinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleSao Paulo2810info:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESPORIGINALS0103-50532017001002038.pdfapplication/pdf303765${dspace.ui.url}/bitstream/11600/57314/1/S0103-50532017001002038.pdfed0ba43008de14d14e9eb1ddd029e5deMD51open accessTEXTS0103-50532017001002038.pdf.txtS0103-50532017001002038.pdf.txtExtracted texttext/plain21372${dspace.ui.url}/bitstream/11600/57314/8/S0103-50532017001002038.pdf.txt6d1ab4894392f5b5419396b788b519dfMD58open accessTHUMBNAILS0103-50532017001002038.pdf.jpgS0103-50532017001002038.pdf.jpgIM Thumbnailimage/jpeg7083${dspace.ui.url}/bitstream/11600/57314/10/S0103-50532017001002038.pdf.jpgcaaa3ce2c5fd5729813f66b57ad068f0MD510open access11600/573142023-06-05 19:24:43.392open accessoai:repositorio.unifesp.br:11600/57314Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-06-05T22:24:43Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.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. [UNIFESP]
Casagrande, Gleison A.
Pizzuti, Lucas
Raminelli, Cristiano [UNIFESP]
author_role author
author2 Rossini, Allan F. C. [UNIFESP]
Casagrande, Gleison A.
Pizzuti, Lucas
Raminelli, Cristiano [UNIFESP]
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Frota, Carlise
Rossini, Allan F. C. [UNIFESP]
Casagrande, Gleison A.
Pizzuti, Lucas
Raminelli, Cristiano [UNIFESP]
dc.subject.eng.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.issued.fl_str_mv 2017
dc.date.accessioned.fl_str_mv 2020-08-04T13:40:08Z
dc.date.available.fl_str_mv 2020-08-04T13:40:08Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv Journal Of The Brazilian Chemical Society. Sao Paulo, v. 28, n. 10, p. 2038-2044, 2017.
dc.identifier.uri.fl_str_mv https://repositorio.unifesp.br/handle/11600/57314
http://dx.doi.org/10.21577/0103-5053.20170035
dc.identifier.issn.none.fl_str_mv 0103-5053
dc.identifier.file.none.fl_str_mv S0103-50532017001002038.pdf
dc.identifier.scielo.none.fl_str_mv S0103-50532017001002038
dc.identifier.doi.none.fl_str_mv 10.21577/0103-5053.20170035
dc.identifier.wos.none.fl_str_mv WOS:000411813200025
identifier_str_mv Journal Of The Brazilian Chemical Society. Sao Paulo, v. 28, n. 10, p. 2038-2044, 2017.
0103-5053
S0103-50532017001002038.pdf
S0103-50532017001002038
10.21577/0103-5053.20170035
WOS:000411813200025
url https://repositorio.unifesp.br/handle/11600/57314
http://dx.doi.org/10.21577/0103-5053.20170035
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Journal Of The Brazilian Chemical Society
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 2038-2044
dc.coverage.none.fl_str_mv Sao Paulo
dc.publisher.none.fl_str_mv Soc Brasileira Quimica
publisher.none.fl_str_mv Soc Brasileira Quimica
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
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