bachelor's at Química com Atribuições em Química Tecnológica from Universidade de São Paulo (2008), bachelor's at Bacharelado em Química from Universidade de São Paulo (2008), master's at Chemistry from Universidade Estadual de Campinas (2011) and doctorate at Chemistry from Universidade Estadual de Campinas (2015). Has experience in Chemistry, focusing on Organic Synthesis (Source: Lattes Curriculum)
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The traditional applied methods for construction and growth of complexity in organic molecules rely on the manipulation of functional groups which are considered reactive, such as, carbonyls, alcohols, amines, and halogenated groups. In contrast, nature routinely uses methods to direct oxidation of C-H bonds, installing oxidized functionalities directly onto complex hydrocarbon framework,…
The use of organic synthesis in the preparation of natural products is of great interest, given the complexity of these compounds and their low availability in nature. For that, the synthetic organic chemists use the environment as inspiration to develop new reactions. In this sense, the objective of this research project is the use of chemical conditions to accomplish the conversion betw…
One of the main challenges in the area of CH bond oxidation is the development of selective reactions due to the ubiquity of this type of bond in organic molecules and its low reactivity. In the case of catalytic systems applied at a late-stage, obtaining chemoselectivity is of great interest. In this sense, the objective of this project is to use complex natural diterpenes as platforms t…
The project aims to investigate a synthetic route to obtain two natural products: 2²,16±,17-trihydroxy-ent-cauran-19-oic acid, and wedelienone, through oxidations of C-H bonds. These products are found, respectively, in Mikania hirsutissima DC and Wedelia Chinensis plants and, as they belong to the kaurene class, we propose to synthesize them from kaurenoic acid. Both routes will be initi…
(Only some records are available in English at this moment)
The selective C-H functionalization of a molecule which already bears others functional groups in its structure has a number of advantages such as, for example, the reduction in number of reaction steps, the reduction of waste generation and the increasy of sinthetic efficiency, since more complex molecules can be prepared in less time. By modifying the structure of a common hydrocarbon i…
The traditional applied methods for construction and growth of complexity in organic molecules rely on the manipulation of functional groups which are considered reactive, such as, carbonyls, alcohols, amines, and halogenated groups. In contrast, nature routinely uses methods to direct oxidation of C-H bonds, installing oxidized functionalities directly onto complex hydrocarbon framework,…
Considering the several challenges for the functionalization of C-H bonds which are very unreactive and have adversities in selectivity with electrophilic reagents, the present research project proposes the use of first period transition metals for metal catalysis as a way of activating methylenic C-H bonds, without the oxidation of the corresponding alcohol to ketone. The first step is t…
(Only some records are available in English at this moment)
| 1 / 1 | Ongoing research grants |
| 4 / 4 | Ongoing scholarships in Brazil |
| 8 / 6 | Completed scholarships in Brazil |
| 13 / 11 | All research grants and scholarships |
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CV Lattes
ORCID