dc.creatorFrota, Carlise
dc.creatorRossini, Allan F. C. [UNIFESP]
dc.creatorCasagrande, Gleison A.
dc.creatorPizzuti, Lucas
dc.creatorRaminelli, Cristiano [UNIFESP]
dc.date.accessioned2020-08-04T13:40:08Z
dc.date.accessioned2023-09-04T18:24:40Z
dc.date.available2020-08-04T13:40:08Z
dc.date.available2023-09-04T18:24:40Z
dc.date.created2020-08-04T13:40:08Z
dc.date.issued2017
dc.identifierJournal Of The Brazilian Chemical Society. Sao Paulo, v. 28, n. 10, p. 2038-2044, 2017.
dc.identifier0103-5053
dc.identifierhttps://repositorio.unifesp.br/handle/11600/57314
dc.identifierS0103-50532017001002038.pdf
dc.identifierS0103-50532017001002038
dc.identifier10.21577/0103-5053.20170035
dc.identifierWOS:000411813200025
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8614294
dc.description.abstractAn 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%.
dc.languageeng
dc.publisherSoc Brasileira Quimica
dc.relationJournal Of The Brazilian Chemical Society
dc.rightsAcesso aberto
dc.subjectelectrophilic iodocyclization
dc.subjectmolecular iodine
dc.subjectdiiodo-functionalized benzo[b] furans
dc.subjectfunctionalized heteroaromatics
dc.subjectdiiodinated compounds
dc.titleSynthesis of Diiodo-Functionalized Benzo[b] furans via Electrophilic Iodocyclization
dc.typeArtigo


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