Estudos visando sínteses totais de substâncias bioativas

Detalhes bibliográficos
Autor(a) principal: Perecim, Givago Prado [UNIFESP]
Data de Publicação: 2020
Tipo de documento: Tese
Idioma: por
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: https://repositorio.unifesp.br/11600/67235
Resumo: A química de benzino tem encontrado aplicações em química orgânica, incluindo sínteses totais de produtos naturais e preparações de materiais funcionais. Neste sentido, 2-(trimetilsilil)aril trifluorometanossulfonatos surgem como uma alternativa importante para a formação de benzino e derivados, sob condições reacionais brandas, ampliando o escopo de aplicações da química de benzino em química orgânica preparativa. Dentro deste contexto, realizamos estudos visando as sínteses totais de substâncias bioativas, a saber: cloridrato de (±)-apomorfina (protótipo aporfinoide); (S)-nuciferina e (R)- nuciferina (alcaloides aporfínicos), bem como morindaparvina A, 1,2- dimetoxiantraquinona, 1-metoxiantraquinona, 2,3-dimetilantraquinona e 2,3- difluorantraquinona (antraquinonas não quirais), com potenciais farmacológicos de interesse, empregando 2-(trimetilsilil)aril triflatos nas correspondentes etapas chaves, sob condições reacionais brandas.
id UFSP_aba9f1e0482607c91f7986a61669b08a
oai_identifier_str oai:repositorio.unifesp.br:11600/67235
network_acronym_str UFSP
network_name_str Repositório Institucional da UNIFESP
repository_id_str 3465
spelling Perecim, Givago Prado [UNIFESP]https://lattes.cnpq.br/5016162413844100http://lattes.cnpq.br/3153931165773039Raminelli, Cristiano [UNIFESP]Diadema2023-03-14T15:13:32Z2023-03-14T15:13:32Z2020-03-06https://repositorio.unifesp.br/11600/67235A química de benzino tem encontrado aplicações em química orgânica, incluindo sínteses totais de produtos naturais e preparações de materiais funcionais. Neste sentido, 2-(trimetilsilil)aril trifluorometanossulfonatos surgem como uma alternativa importante para a formação de benzino e derivados, sob condições reacionais brandas, ampliando o escopo de aplicações da química de benzino em química orgânica preparativa. Dentro deste contexto, realizamos estudos visando as sínteses totais de substâncias bioativas, a saber: cloridrato de (±)-apomorfina (protótipo aporfinoide); (S)-nuciferina e (R)- nuciferina (alcaloides aporfínicos), bem como morindaparvina A, 1,2- dimetoxiantraquinona, 1-metoxiantraquinona, 2,3-dimetilantraquinona e 2,3- difluorantraquinona (antraquinonas não quirais), com potenciais farmacológicos de interesse, empregando 2-(trimetilsilil)aril triflatos nas correspondentes etapas chaves, sob condições reacionais brandas.Benzene chemistry has found applications in organic chemistry, including total natural product syntheses and functional material preparations. In this sense, 2-(trimethylsilyl)aryl trifluoromethanesulfonates emerge as an important alternative for the formation of benzene and derivatives, under mild reaction conditions, expanding the scope of applications of benzene chemistry in preparative organic chemistry. Within this context, we carried out studies aiming at the total synthesis of bioactive substances, namely: (±)-apomorphine hydrochloride (aporphinoid prototype); (S)-nuciferin and (R)-nuciferin (aporphine alkaloids), as well as morindaparvin A, 1,2-dimethoxyanthraquinone, 1-methoxyanthraquinone, 2,3-dimethylanthraquinone and 2,3-difluoroanthraquinone (non-chiral anthraquinones), with potential pharmacological studies of interest, employing 2-(trimethylsilyl)aryl triflates in the corresponding key steps, under mild reaction conditions.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)221 f.porUniversidade Federal de São PauloQuímica de benzinoSínteses totaisSubstâncias bioativasAlcaloidesAntraquinonasBenzyne chemistryTotal synthesesBioactive substancesAlkaloidsAnthraquinonesEstudos visando sínteses totais de substâncias bioativasStudies aimed at total syntheses of substances bioactiveinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESPInstituto de Ciências Ambientais, Químicas e Farmacêuticas (ICAQF)Biologia QuímicaBiologia QuímicaBiologia Química de Produtos Naturais e SintéticosORIGINALTESE Doutorado - Givago Perecim.pdfTESE Doutorado - Givago Perecim.pdfTese de Doutoradoapplication/pdf93362794${dspace.ui.url}/bitstream/11600/67235/5/TESE%20Doutorado%20-%20Givago%20Perecim.pdfce9d2e3f142b2f2f4c190d1b9c54ff64MD55open accessLICENSElicense.txtlicense.txttext/plain; charset=utf-85805${dspace.ui.url}/bitstream/11600/67235/6/license.txt76b66fed910c8d19644a2bc51255b95aMD56open accessTHUMBNAILTESE Doutorado - Givago Perecim.pdf.jpgTESE Doutorado - Givago Perecim.pdf.jpgIM Thumbnailimage/jpeg4057${dspace.ui.url}/bitstream/11600/67235/7/TESE%20Doutorado%20-%20Givago%20Perecim.pdf.jpg154e615ae45b872937cfcdf5cd37f93bMD57open access11600/672352023-10-30 01:01:48.921open accessoai:repositorio.unifesp.br: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ório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-10-30T04:01:48Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.pt_BR.fl_str_mv Estudos visando sínteses totais de substâncias bioativas
dc.title.alternative.pt_BR.fl_str_mv Studies aimed at total syntheses of substances bioactive
title Estudos visando sínteses totais de substâncias bioativas
spellingShingle Estudos visando sínteses totais de substâncias bioativas
Perecim, Givago Prado [UNIFESP]
Química de benzino
Sínteses totais
Substâncias bioativas
Alcaloides
Antraquinonas
Benzyne chemistry
Total syntheses
Bioactive substances
Alkaloids
Anthraquinones
title_short Estudos visando sínteses totais de substâncias bioativas
title_full Estudos visando sínteses totais de substâncias bioativas
title_fullStr Estudos visando sínteses totais de substâncias bioativas
title_full_unstemmed Estudos visando sínteses totais de substâncias bioativas
title_sort Estudos visando sínteses totais de substâncias bioativas
author Perecim, Givago Prado [UNIFESP]
author_facet Perecim, Givago Prado [UNIFESP]
author_role author
dc.contributor.authorLattes.pt_BR.fl_str_mv https://lattes.cnpq.br/5016162413844100
dc.contributor.advisorLattes.pt_BR.fl_str_mv http://lattes.cnpq.br/3153931165773039
dc.contributor.author.fl_str_mv Perecim, Givago Prado [UNIFESP]
dc.contributor.advisor1.fl_str_mv Raminelli, Cristiano [UNIFESP]
contributor_str_mv Raminelli, Cristiano [UNIFESP]
dc.subject.por.fl_str_mv Química de benzino
Sínteses totais
Substâncias bioativas
Alcaloides
Antraquinonas
topic Química de benzino
Sínteses totais
Substâncias bioativas
Alcaloides
Antraquinonas
Benzyne chemistry
Total syntheses
Bioactive substances
Alkaloids
Anthraquinones
dc.subject.eng.fl_str_mv Benzyne chemistry
Total syntheses
Bioactive substances
Alkaloids
Anthraquinones
description A química de benzino tem encontrado aplicações em química orgânica, incluindo sínteses totais de produtos naturais e preparações de materiais funcionais. Neste sentido, 2-(trimetilsilil)aril trifluorometanossulfonatos surgem como uma alternativa importante para a formação de benzino e derivados, sob condições reacionais brandas, ampliando o escopo de aplicações da química de benzino em química orgânica preparativa. Dentro deste contexto, realizamos estudos visando as sínteses totais de substâncias bioativas, a saber: cloridrato de (±)-apomorfina (protótipo aporfinoide); (S)-nuciferina e (R)- nuciferina (alcaloides aporfínicos), bem como morindaparvina A, 1,2- dimetoxiantraquinona, 1-metoxiantraquinona, 2,3-dimetilantraquinona e 2,3- difluorantraquinona (antraquinonas não quirais), com potenciais farmacológicos de interesse, empregando 2-(trimetilsilil)aril triflatos nas correspondentes etapas chaves, sob condições reacionais brandas.
publishDate 2020
dc.date.issued.fl_str_mv 2020-03-06
dc.date.accessioned.fl_str_mv 2023-03-14T15:13:32Z
dc.date.available.fl_str_mv 2023-03-14T15:13:32Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://repositorio.unifesp.br/11600/67235
url https://repositorio.unifesp.br/11600/67235
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 221 f.
dc.coverage.spatial.pt_BR.fl_str_mv Diadema
dc.publisher.none.fl_str_mv Universidade Federal de São Paulo
publisher.none.fl_str_mv Universidade Federal de São Paulo
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
bitstream.url.fl_str_mv ${dspace.ui.url}/bitstream/11600/67235/5/TESE%20Doutorado%20-%20Givago%20Perecim.pdf
${dspace.ui.url}/bitstream/11600/67235/6/license.txt
${dspace.ui.url}/bitstream/11600/67235/7/TESE%20Doutorado%20-%20Givago%20Perecim.pdf.jpg
bitstream.checksum.fl_str_mv ce9d2e3f142b2f2f4c190d1b9c54ff64
76b66fed910c8d19644a2bc51255b95a
154e615ae45b872937cfcdf5cd37f93b
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv
_version_ 1802764259105439744

Registros relacionados