Tecnologias em fluxo contínuo de compostos cicloeptânicos derivados da (R)-(–)-carvona e do fragmento C23-C31 usado na síntese total dos policetídeos spirangien A metil éster e spirodienal A

Detalhes bibliográficos
Autor(a) principal: Alves, Leandro de Carvalho
Data de Publicação: 2015
Tipo de documento: Tese
Idioma: por
Título da fonte: Repositório Institucional da UFSCAR
Texto Completo: https://repositorio.ufscar.br/handle/ufscar/10725
Resumo: Continuous flow technology of cycloheptanic compounds derived from (R)-(–)-carvone and the C23-C31 fragment used in the total synthesis of spirangien A methyl ester and spirodienal A polyketides” In the first part of this thesis is described the improvement and development of two synthetic routes to the cycloheptenone 73, in the deca-gram scale, from the monoterpene (R)-(–)-carvone (58). Were developed reactions in the continuous flow mode to accelerate and increase the scale production of 73, and thus avoiding chemical logistics issues. Sharing the principle of the diversity oriented synthesis and taking advantage from the cycloheptanic chiron flexibility, were developed α-carbonyl alkylations followed by catalysis with transition metal, to get, in a fast way, structurally diverse compounds such as spiro 74, guaiane type 75, xathane 76 and the tris-ketal compound 78. The second part of this thesis encompasses some results of our collaboration with Prof. Steven V. Ley CBE FRS and deals with the synthesis acceleration of the fragment 145 through the usage of continuous flow processes. The compound 145 is an advanced synthetic intermediate for the spirangien A (79), spirangien A methyl ester (80) and spirodienal A (81) syntheses, which are on matter at the Prof. Ley`s group. xxiii
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spelling Alves, Leandro de CarvalhoBrocksom, Timothy Johnhttp://lattes.cnpq.br/7055452150201902http://lattes.cnpq.br/2992788465442455e5e0b421-37f4-43ad-8cac-f169b64178e42018-11-28T12:04:01Z2018-11-28T12:04:01Z2015-05-20ALVES, Leandro de Carvalho. Tecnologias em fluxo contínuo de compostos cicloeptânicos derivados da (R)-(–)-carvona e do fragmento C23-C31 usado na síntese total dos policetídeos spirangien A metil éster e spirodienal A. 2015. Tese (Doutorado em Química) – Universidade Federal de São Carlos, São Carlos, 2015. Disponível em: https://repositorio.ufscar.br/handle/ufscar/10725.https://repositorio.ufscar.br/handle/ufscar/10725Continuous flow technology of cycloheptanic compounds derived from (R)-(–)-carvone and the C23-C31 fragment used in the total synthesis of spirangien A methyl ester and spirodienal A polyketides” In the first part of this thesis is described the improvement and development of two synthetic routes to the cycloheptenone 73, in the deca-gram scale, from the monoterpene (R)-(–)-carvone (58). Were developed reactions in the continuous flow mode to accelerate and increase the scale production of 73, and thus avoiding chemical logistics issues. Sharing the principle of the diversity oriented synthesis and taking advantage from the cycloheptanic chiron flexibility, were developed α-carbonyl alkylations followed by catalysis with transition metal, to get, in a fast way, structurally diverse compounds such as spiro 74, guaiane type 75, xathane 76 and the tris-ketal compound 78. The second part of this thesis encompasses some results of our collaboration with Prof. Steven V. Ley CBE FRS and deals with the synthesis acceleration of the fragment 145 through the usage of continuous flow processes. The compound 145 is an advanced synthetic intermediate for the spirangien A (79), spirangien A methyl ester (80) and spirodienal A (81) syntheses, which are on matter at the Prof. Ley`s group. xxiiiTecnologias em fluxo contínuo de compostos cicloeptânicos derivados da (R)-(–)-carvona e do fragmento C23-C31 usado na síntese total dos policetídeos spirangien A metil éster e spirodienal A” A primeira parte deste trabalho descreve o aprimoramento e/ou desenvolvimento de duas rotas sintéticas para a obtenção da cicloeptenona 73, na escala decagrama, a partir do monoterpeno (R)-(–)-carvona (58). Foram desenvolvidas reações em modo fluxo contínuo para acelerar e aumentar a produção de 73 evitando problemas de logística química. Compartilhando do princípio da síntese dirigida para a diversidade (DOS) e aproveitando a versatilidade do quíron cicloeptânico, foram desenvolvidas reações de alquilação α-carbonílicas seguidas de catálise com metais de transição para obter, de maneira rápida, compostos estruturalmente diversos como compostos espiro 74, do tipo guaiano 75, xantano 76 e o tris-cetal 78. A segunda parte do trabalho descreve alguns resultados da nossa colaboração com o Prof. Steven V. Ley CBE FRS e trata da aceleração da síntese do fragmento 145 através do uso de tecnologias em fluxo contínuo. O composto é um intermediário avançado na síntese dos produtos naturais spirangien A (79), spirangien A metil éster (80) e spirodienal A (81), atualmente em desenvolvimento no grupo do Prof. Ley. xxiConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)CNPq: 245949/2012-7FAPESP: 2014/12001-4porUniversidade Federal de São CarlosCâmpus São CarlosPrograma de Pós-Graduação em Química - PPGQUFSCarRotas sintéticasCicloeptonaEscala decagramaMonoterpenoCarvonaReação de alquilaçãoSynthetic routesCycloheptenoneDeca-gram scaleMonoterpeneCarvoneReactions alkylationsCIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA ORGANICA::SINTESE ORGANICATecnologias em fluxo contínuo de compostos cicloeptânicos derivados da (R)-(–)-carvona e do fragmento C23-C31 usado na síntese total dos policetídeos spirangien A metil éster e spirodienal AContinuous flow technology of cycloheptanic compounds derived from (R)-(–)-carvone and the C23-C31 fragment used in the total synthesis of spirangien A methyl ester and spirodienal A polyketidesinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisOnline6006003f6498ab-9d48-447f-8154-7904dbbe8158info:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFSCARinstname:Universidade Federal de São Carlos (UFSCAR)instacron:UFSCARORIGINALTeseLCA.pdfTeseLCA.pdfapplication/pdf11985180https://repositorio.ufscar.br/bitstream/ufscar/10725/1/TeseLCA.pdf507856066c863594156e9884895b9bdcMD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81957https://repositorio.ufscar.br/bitstream/ufscar/10725/2/license.txtae0398b6f8b235e40ad82cba6c50031dMD52TEXTTeseLCA.pdf.txtTeseLCA.pdf.txtExtracted texttext/plain262533https://repositorio.ufscar.br/bitstream/ufscar/10725/3/TeseLCA.pdf.txtaefd17eb2913360c3a0eb80d5ac6f508MD53THUMBNAILTeseLCA.pdf.jpgTeseLCA.pdf.jpgIM Thumbnailimage/jpeg9636https://repositorio.ufscar.br/bitstream/ufscar/10725/4/TeseLCA.pdf.jpg4e960b3dfcfbc62f71bddc6c2686fdf3MD54ufscar/107252023-09-18 18:31:18.161oai:repositorio.ufscar.br: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Repositório InstitucionalPUBhttps://repositorio.ufscar.br/oai/requestopendoar:43222023-09-18T18:31:18Repositório Institucional da UFSCAR - Universidade Federal de São Carlos (UFSCAR)false
dc.title.por.fl_str_mv Tecnologias em fluxo contínuo de compostos cicloeptânicos derivados da (R)-(–)-carvona e do fragmento C23-C31 usado na síntese total dos policetídeos spirangien A metil éster e spirodienal A
dc.title.alternative.eng.fl_str_mv Continuous flow technology of cycloheptanic compounds derived from (R)-(–)-carvone and the C23-C31 fragment used in the total synthesis of spirangien A methyl ester and spirodienal A polyketides
title Tecnologias em fluxo contínuo de compostos cicloeptânicos derivados da (R)-(–)-carvona e do fragmento C23-C31 usado na síntese total dos policetídeos spirangien A metil éster e spirodienal A
spellingShingle Tecnologias em fluxo contínuo de compostos cicloeptânicos derivados da (R)-(–)-carvona e do fragmento C23-C31 usado na síntese total dos policetídeos spirangien A metil éster e spirodienal A
Alves, Leandro de Carvalho
Rotas sintéticas
Cicloeptona
Escala decagrama
Monoterpeno
Carvona
Reação de alquilação
Synthetic routes
Cycloheptenone
Deca-gram scale
Monoterpene
Carvone
Reactions alkylations
CIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA ORGANICA::SINTESE ORGANICA
title_short Tecnologias em fluxo contínuo de compostos cicloeptânicos derivados da (R)-(–)-carvona e do fragmento C23-C31 usado na síntese total dos policetídeos spirangien A metil éster e spirodienal A
title_full Tecnologias em fluxo contínuo de compostos cicloeptânicos derivados da (R)-(–)-carvona e do fragmento C23-C31 usado na síntese total dos policetídeos spirangien A metil éster e spirodienal A
title_fullStr Tecnologias em fluxo contínuo de compostos cicloeptânicos derivados da (R)-(–)-carvona e do fragmento C23-C31 usado na síntese total dos policetídeos spirangien A metil éster e spirodienal A
title_full_unstemmed Tecnologias em fluxo contínuo de compostos cicloeptânicos derivados da (R)-(–)-carvona e do fragmento C23-C31 usado na síntese total dos policetídeos spirangien A metil éster e spirodienal A
title_sort Tecnologias em fluxo contínuo de compostos cicloeptânicos derivados da (R)-(–)-carvona e do fragmento C23-C31 usado na síntese total dos policetídeos spirangien A metil éster e spirodienal A
author Alves, Leandro de Carvalho
author_facet Alves, Leandro de Carvalho
author_role author
dc.contributor.authorlattes.por.fl_str_mv http://lattes.cnpq.br/2992788465442455
dc.contributor.author.fl_str_mv Alves, Leandro de Carvalho
dc.contributor.advisor1.fl_str_mv Brocksom, Timothy John
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/7055452150201902
dc.contributor.authorID.fl_str_mv e5e0b421-37f4-43ad-8cac-f169b64178e4
contributor_str_mv Brocksom, Timothy John
dc.subject.por.fl_str_mv Rotas sintéticas
Cicloeptona
Escala decagrama
Monoterpeno
Carvona
Reação de alquilação
topic Rotas sintéticas
Cicloeptona
Escala decagrama
Monoterpeno
Carvona
Reação de alquilação
Synthetic routes
Cycloheptenone
Deca-gram scale
Monoterpene
Carvone
Reactions alkylations
CIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA ORGANICA::SINTESE ORGANICA
dc.subject.eng.fl_str_mv Synthetic routes
Cycloheptenone
Deca-gram scale
Monoterpene
Carvone
Reactions alkylations
dc.subject.cnpq.fl_str_mv CIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA ORGANICA::SINTESE ORGANICA
description Continuous flow technology of cycloheptanic compounds derived from (R)-(–)-carvone and the C23-C31 fragment used in the total synthesis of spirangien A methyl ester and spirodienal A polyketides” In the first part of this thesis is described the improvement and development of two synthetic routes to the cycloheptenone 73, in the deca-gram scale, from the monoterpene (R)-(–)-carvone (58). Were developed reactions in the continuous flow mode to accelerate and increase the scale production of 73, and thus avoiding chemical logistics issues. Sharing the principle of the diversity oriented synthesis and taking advantage from the cycloheptanic chiron flexibility, were developed α-carbonyl alkylations followed by catalysis with transition metal, to get, in a fast way, structurally diverse compounds such as spiro 74, guaiane type 75, xathane 76 and the tris-ketal compound 78. The second part of this thesis encompasses some results of our collaboration with Prof. Steven V. Ley CBE FRS and deals with the synthesis acceleration of the fragment 145 through the usage of continuous flow processes. The compound 145 is an advanced synthetic intermediate for the spirangien A (79), spirangien A methyl ester (80) and spirodienal A (81) syntheses, which are on matter at the Prof. Ley`s group. xxiii
publishDate 2015
dc.date.issued.fl_str_mv 2015-05-20
dc.date.accessioned.fl_str_mv 2018-11-28T12:04:01Z
dc.date.available.fl_str_mv 2018-11-28T12:04:01Z
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.citation.fl_str_mv ALVES, Leandro de Carvalho. Tecnologias em fluxo contínuo de compostos cicloeptânicos derivados da (R)-(–)-carvona e do fragmento C23-C31 usado na síntese total dos policetídeos spirangien A metil éster e spirodienal A. 2015. Tese (Doutorado em Química) – Universidade Federal de São Carlos, São Carlos, 2015. Disponível em: https://repositorio.ufscar.br/handle/ufscar/10725.
dc.identifier.uri.fl_str_mv https://repositorio.ufscar.br/handle/ufscar/10725
identifier_str_mv ALVES, Leandro de Carvalho. Tecnologias em fluxo contínuo de compostos cicloeptânicos derivados da (R)-(–)-carvona e do fragmento C23-C31 usado na síntese total dos policetídeos spirangien A metil éster e spirodienal A. 2015. Tese (Doutorado em Química) – Universidade Federal de São Carlos, São Carlos, 2015. Disponível em: https://repositorio.ufscar.br/handle/ufscar/10725.
url https://repositorio.ufscar.br/handle/ufscar/10725
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Câmpus São Carlos
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Química - PPGQ
dc.publisher.initials.fl_str_mv UFSCar
publisher.none.fl_str_mv Universidade Federal de São Carlos
Câmpus São Carlos
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