Suzuki-Miyaura coupling between 3-Iodolawsone and arylboronic acids. Synthesis of lapachol analogues with antineoplastic and antileishmanial activities

Detalhes bibliográficos
Autor(a) principal: Gomes, Sara L. S.
Data de Publicação: 2017
Outros Autores: Militão, Gardenia C. G., Costa, Arinice M., Pessoa, Cláudia Ó., Costa-Lotufo, Letícia V., Torres-Santos, Eduardo C., Costa, Paulo R. R., Silva, Alcides J. M. da, Cunha-Junior, Edézio F.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da Universidade Federal do Ceará (UFC)
Texto Completo: http://www.repositorio.ufc.br/handle/riufc/27266
Resumo: A series of 2-hydroxy-3-arylnaphthalene-1,4-diones (3-aryllawsones) were synthesized by Suzuki-Miyaura cross coupling reaction of 3-iodolawsone with arylboronic acids/esters. The hydroxylated resulting products were transformed into their corresponding N , N -diethyl carbamates. The antineoplastic and antileishmanial activities of the compounds were evaluated and compared with lapachol and its carbamate, providing promising results.
id UFC-7_977504fc317b3d79fd53391c00b868e5
oai_identifier_str oai:repositorio.ufc.br:riufc/27266
network_acronym_str UFC-7
network_name_str Repositório Institucional da Universidade Federal do Ceará (UFC)
repository_id_str
spelling Suzuki-Miyaura coupling between 3-Iodolawsone and arylboronic acids. Synthesis of lapachol analogues with antineoplastic and antileishmanial activitiesQuinonesQuinonasLevopropoxifenoA series of 2-hydroxy-3-arylnaphthalene-1,4-diones (3-aryllawsones) were synthesized by Suzuki-Miyaura cross coupling reaction of 3-iodolawsone with arylboronic acids/esters. The hydroxylated resulting products were transformed into their corresponding N , N -diethyl carbamates. The antineoplastic and antileishmanial activities of the compounds were evaluated and compared with lapachol and its carbamate, providing promising results.Journal of the Brazilian Chemical Society2017-11-08T14:22:35Z2017-11-08T14:22:35Z2017info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfGOMES, S. L. S. et al. Suzuki-Miyaura coupling between 3-Iodolawsone and Arylboronic acids. Synthesis of Lapachol analogues with antineoplastic and antileishmanial activities. Journal of the Brazilian Chemical Society, São Paulo, v. 28, n. 8, p. 1573-1584, 2017.0103-5053http://www.repositorio.ufc.br/handle/riufc/27266Gomes, Sara L. S.Militão, Gardenia C. G.Costa, Arinice M.Pessoa, Cláudia Ó.Costa-Lotufo, Letícia V.Torres-Santos, Eduardo C.Costa, Paulo R. R.Silva, Alcides J. M. daCunha-Junior, Edézio F.engreponame:Repositório Institucional da Universidade Federal do Ceará (UFC)instname:Universidade Federal do Ceará (UFC)instacron:UFCinfo:eu-repo/semantics/openAccess2019-10-17T17:17:32Zoai:repositorio.ufc.br:riufc/27266Repositório InstitucionalPUBhttp://www.repositorio.ufc.br/ri-oai/requestbu@ufc.br || repositorio@ufc.bropendoar:2024-09-11T18:42:55.338589Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)false
dc.title.none.fl_str_mv Suzuki-Miyaura coupling between 3-Iodolawsone and arylboronic acids. Synthesis of lapachol analogues with antineoplastic and antileishmanial activities
title Suzuki-Miyaura coupling between 3-Iodolawsone and arylboronic acids. Synthesis of lapachol analogues with antineoplastic and antileishmanial activities
spellingShingle Suzuki-Miyaura coupling between 3-Iodolawsone and arylboronic acids. Synthesis of lapachol analogues with antineoplastic and antileishmanial activities
Gomes, Sara L. S.
Quinones
Quinonas
Levopropoxifeno
title_short Suzuki-Miyaura coupling between 3-Iodolawsone and arylboronic acids. Synthesis of lapachol analogues with antineoplastic and antileishmanial activities
title_full Suzuki-Miyaura coupling between 3-Iodolawsone and arylboronic acids. Synthesis of lapachol analogues with antineoplastic and antileishmanial activities
title_fullStr Suzuki-Miyaura coupling between 3-Iodolawsone and arylboronic acids. Synthesis of lapachol analogues with antineoplastic and antileishmanial activities
title_full_unstemmed Suzuki-Miyaura coupling between 3-Iodolawsone and arylboronic acids. Synthesis of lapachol analogues with antineoplastic and antileishmanial activities
title_sort Suzuki-Miyaura coupling between 3-Iodolawsone and arylboronic acids. Synthesis of lapachol analogues with antineoplastic and antileishmanial activities
author Gomes, Sara L. S.
author_facet Gomes, Sara L. S.
Militão, Gardenia C. G.
Costa, Arinice M.
Pessoa, Cláudia Ó.
Costa-Lotufo, Letícia V.
Torres-Santos, Eduardo C.
Costa, Paulo R. R.
Silva, Alcides J. M. da
Cunha-Junior, Edézio F.
author_role author
author2 Militão, Gardenia C. G.
Costa, Arinice M.
Pessoa, Cláudia Ó.
Costa-Lotufo, Letícia V.
Torres-Santos, Eduardo C.
Costa, Paulo R. R.
Silva, Alcides J. M. da
Cunha-Junior, Edézio F.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Gomes, Sara L. S.
Militão, Gardenia C. G.
Costa, Arinice M.
Pessoa, Cláudia Ó.
Costa-Lotufo, Letícia V.
Torres-Santos, Eduardo C.
Costa, Paulo R. R.
Silva, Alcides J. M. da
Cunha-Junior, Edézio F.
dc.subject.por.fl_str_mv Quinones
Quinonas
Levopropoxifeno
topic Quinones
Quinonas
Levopropoxifeno
description A series of 2-hydroxy-3-arylnaphthalene-1,4-diones (3-aryllawsones) were synthesized by Suzuki-Miyaura cross coupling reaction of 3-iodolawsone with arylboronic acids/esters. The hydroxylated resulting products were transformed into their corresponding N , N -diethyl carbamates. The antineoplastic and antileishmanial activities of the compounds were evaluated and compared with lapachol and its carbamate, providing promising results.
publishDate 2017
dc.date.none.fl_str_mv 2017-11-08T14:22:35Z
2017-11-08T14:22:35Z
2017
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.uri.fl_str_mv GOMES, S. L. S. et al. Suzuki-Miyaura coupling between 3-Iodolawsone and Arylboronic acids. Synthesis of Lapachol analogues with antineoplastic and antileishmanial activities. Journal of the Brazilian Chemical Society, São Paulo, v. 28, n. 8, p. 1573-1584, 2017.
0103-5053
http://www.repositorio.ufc.br/handle/riufc/27266
identifier_str_mv GOMES, S. L. S. et al. Suzuki-Miyaura coupling between 3-Iodolawsone and Arylboronic acids. Synthesis of Lapachol analogues with antineoplastic and antileishmanial activities. Journal of the Brazilian Chemical Society, São Paulo, v. 28, n. 8, p. 1573-1584, 2017.
0103-5053
url http://www.repositorio.ufc.br/handle/riufc/27266
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Journal of the Brazilian Chemical Society
publisher.none.fl_str_mv Journal of the Brazilian Chemical Society
dc.source.none.fl_str_mv reponame:Repositório Institucional da Universidade Federal do Ceará (UFC)
instname:Universidade Federal do Ceará (UFC)
instacron:UFC
instname_str Universidade Federal do Ceará (UFC)
instacron_str UFC
institution UFC
reponame_str Repositório Institucional da Universidade Federal do Ceará (UFC)
collection Repositório Institucional da Universidade Federal do Ceará (UFC)
repository.name.fl_str_mv Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)
repository.mail.fl_str_mv bu@ufc.br || repositorio@ufc.br
_version_ 1813028917365178368