CV Lattes
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Universidade de São Paulo (USP). Instituto de Química (IQ) (Institutional affiliation from the last research proposal) Birthplace: Brazil
graduation at Bacharelado em Química from Universidade Federal da Bahia (2010), master's at Chemistry from Universidade Estadual de Campinas (2012) and doctorate at Chemistry from Universidade Estadual de Campinas (2017). Has experience in Chemistry, focusing on Chemistry, acting on the following subjects: cascade reactions, aza-ciclização, enaminonas, iridium photocatalysts and allopumiliotoxinas. (Source: Lattes Curriculum)
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Until my appointment, the Institute of Chemistry at USP had three research groups active in the field of Organic Synthesis: the group of Prof. Bruno Paz, dedicated to the study of Asymmetric Catalysis; the group of Prof. Alcindo dos Santos, focused on the Synthesis of Sulfur, Selenium, and Tellurium Compounds; and the group of Prof. Leandro Helguera, oriented toward Sustainability in Mole…
The development of sustainable synthetic strategies that rapidly achieve the synthesis of (new) molecules with pharmacological or technological interest is one of the biggest challenges in the contemporaneous organic synthesis. The use of light to promote chemical transformations consist in great appeal in this regard, since light is the cleanest source of energy, and the sunlight stands…
This PhD project has as main proposal exploiting the synthetic potentiality of intermediates, prepared from Morita-Baylis-Hillman adducts, as substrate for an intramolecular nucleophilic substitution or benzoinic condensation mediated by N-heterocyclic carbenes. The cyclic product obtained in the intramolecular nucleophilc substitution step will be used as substrate for the stereoselectiv…
The proposed postdoctoral stage project consists in the development of strategies for dicarbofunctionalization of deactivated olefins using carbon dioxide and radical precursors. Initially, a nickel catalyzed redox strategy of trifluoromethylcarboxylation, using (2,2,2-trifluoroacetoxy) pyridinium trifluoroacetate as a precursor of the trifluoromethyl radical will be investigated. This st…
The project consists on a methodological study of two transformations involving Indolizines obtained from Morita-Baylis-Hillman adducts. They are: an asymmetric transfer hydrogenation reaction and an asymmetric Friedel-Crafts alkylation , both catalyzed by chiral phosphoric acids derived from BINOL. The Indolizines are interesting building blocks, since they can be converted to compounds …
| 1 / 1 | Ongoing grants |
| 2 / 2 | Completed scholarships in Brazil |
| 2 / 2 | Completed scholarships abroad |
| 5 / 5 | All research grants and scholarships |
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