New Synthetic Routes for the Valorization of Easily Accessible Bio-renewable Resources

Detalhes bibliográficos
Autor(a) principal: Cavaca, Lídia Alexandra Santos
Data de Publicação: 2017
Tipo de documento: Dissertação
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10362/24092
Resumo: The olive tree (Olea europaea) is a natural source of a diversity of phenolic compounds, including secoiridoids. Oleuropein is the major secoiridoid found in olive tree and other plants from the Oleaceae family. It is found in olive fruit and small branches, although exists in higher amounts in olive leaves. Olive leaves are by-products from olive oil industries, and have no practical applications, being considered an easily accessible bio-renewable resource of oleuropein. The molecular structure of oleuropein is divided in three subunits: hydroxytyrosol, glucose and monoterpene moieties. The glucose unit confers solubility in water, while hydroxytyrosol is responsible for most of its biological properties. However, the monoterpene moiety is more interesting in chemical reactivity point of view, having two asymmetric centers and seven potential reactive positions, available for synthetic modifications. This work consisted on the extraction and isolation of oleuropein from olive leaves and the study of semi-synthetic transformations in order to obtain new derivatives, by removal of the glucose and hydroxytyrosol moieties, and modifications at monoterpene core, focusing on a complete study of the methanolysis reaction of oleuropein in acidic conditions. It was based on a screening of protic acids and acidic resins and a study of the temperature effect, with quantitative analysis by HPLC-UV, complemented by a mechanistic study of the reaction. A continuous flow approach was also performed, with positive results. In one pot, the methanolysis reaction allowed several transformations on the molecular structure of oleuropein, with formation of a compound with reported antiviral activity and used as precursor on an anti-hypertensive drug synthesis, as well as compounds with potential to be used in the synthesis of derivatives with novel pharmaceutical properties and other additional interest.
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spelling New Synthetic Routes for the Valorization of Easily Accessible Bio-renewable ResourcesOleuropeinOlive leavesBiomassMethanolysisCatalysisDomínio/Área Científica::Engenharia e Tecnologia::Engenharia QuímicaThe olive tree (Olea europaea) is a natural source of a diversity of phenolic compounds, including secoiridoids. Oleuropein is the major secoiridoid found in olive tree and other plants from the Oleaceae family. It is found in olive fruit and small branches, although exists in higher amounts in olive leaves. Olive leaves are by-products from olive oil industries, and have no practical applications, being considered an easily accessible bio-renewable resource of oleuropein. The molecular structure of oleuropein is divided in three subunits: hydroxytyrosol, glucose and monoterpene moieties. The glucose unit confers solubility in water, while hydroxytyrosol is responsible for most of its biological properties. However, the monoterpene moiety is more interesting in chemical reactivity point of view, having two asymmetric centers and seven potential reactive positions, available for synthetic modifications. This work consisted on the extraction and isolation of oleuropein from olive leaves and the study of semi-synthetic transformations in order to obtain new derivatives, by removal of the glucose and hydroxytyrosol moieties, and modifications at monoterpene core, focusing on a complete study of the methanolysis reaction of oleuropein in acidic conditions. It was based on a screening of protic acids and acidic resins and a study of the temperature effect, with quantitative analysis by HPLC-UV, complemented by a mechanistic study of the reaction. A continuous flow approach was also performed, with positive results. In one pot, the methanolysis reaction allowed several transformations on the molecular structure of oleuropein, with formation of a compound with reported antiviral activity and used as precursor on an anti-hypertensive drug synthesis, as well as compounds with potential to be used in the synthesis of derivatives with novel pharmaceutical properties and other additional interest.Afonso, CarlosRodrigues, CatarinaRUNCavaca, Lídia Alexandra Santos2017-10-12T14:09:15Z2017-092017-102017-09-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://hdl.handle.net/10362/24092enginfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-03-11T04:12:27Zoai:run.unl.pt:10362/24092Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:27:58.737352Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv New Synthetic Routes for the Valorization of Easily Accessible Bio-renewable Resources
title New Synthetic Routes for the Valorization of Easily Accessible Bio-renewable Resources
spellingShingle New Synthetic Routes for the Valorization of Easily Accessible Bio-renewable Resources
Cavaca, Lídia Alexandra Santos
Oleuropein
Olive leaves
Biomass
Methanolysis
Catalysis
Domínio/Área Científica::Engenharia e Tecnologia::Engenharia Química
title_short New Synthetic Routes for the Valorization of Easily Accessible Bio-renewable Resources
title_full New Synthetic Routes for the Valorization of Easily Accessible Bio-renewable Resources
title_fullStr New Synthetic Routes for the Valorization of Easily Accessible Bio-renewable Resources
title_full_unstemmed New Synthetic Routes for the Valorization of Easily Accessible Bio-renewable Resources
title_sort New Synthetic Routes for the Valorization of Easily Accessible Bio-renewable Resources
author Cavaca, Lídia Alexandra Santos
author_facet Cavaca, Lídia Alexandra Santos
author_role author
dc.contributor.none.fl_str_mv Afonso, Carlos
Rodrigues, Catarina
RUN
dc.contributor.author.fl_str_mv Cavaca, Lídia Alexandra Santos
dc.subject.por.fl_str_mv Oleuropein
Olive leaves
Biomass
Methanolysis
Catalysis
Domínio/Área Científica::Engenharia e Tecnologia::Engenharia Química
topic Oleuropein
Olive leaves
Biomass
Methanolysis
Catalysis
Domínio/Área Científica::Engenharia e Tecnologia::Engenharia Química
description The olive tree (Olea europaea) is a natural source of a diversity of phenolic compounds, including secoiridoids. Oleuropein is the major secoiridoid found in olive tree and other plants from the Oleaceae family. It is found in olive fruit and small branches, although exists in higher amounts in olive leaves. Olive leaves are by-products from olive oil industries, and have no practical applications, being considered an easily accessible bio-renewable resource of oleuropein. The molecular structure of oleuropein is divided in three subunits: hydroxytyrosol, glucose and monoterpene moieties. The glucose unit confers solubility in water, while hydroxytyrosol is responsible for most of its biological properties. However, the monoterpene moiety is more interesting in chemical reactivity point of view, having two asymmetric centers and seven potential reactive positions, available for synthetic modifications. This work consisted on the extraction and isolation of oleuropein from olive leaves and the study of semi-synthetic transformations in order to obtain new derivatives, by removal of the glucose and hydroxytyrosol moieties, and modifications at monoterpene core, focusing on a complete study of the methanolysis reaction of oleuropein in acidic conditions. It was based on a screening of protic acids and acidic resins and a study of the temperature effect, with quantitative analysis by HPLC-UV, complemented by a mechanistic study of the reaction. A continuous flow approach was also performed, with positive results. In one pot, the methanolysis reaction allowed several transformations on the molecular structure of oleuropein, with formation of a compound with reported antiviral activity and used as precursor on an anti-hypertensive drug synthesis, as well as compounds with potential to be used in the synthesis of derivatives with novel pharmaceutical properties and other additional interest.
publishDate 2017
dc.date.none.fl_str_mv 2017-10-12T14:09:15Z
2017-09
2017-10
2017-09-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
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url http://hdl.handle.net/10362/24092
dc.language.iso.fl_str_mv eng
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instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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