A5056935415- Luminescence and Fluorescent Materials
- Molecular Sensors and Ion Detection
- Porphyrin and Phthalocyanine Chemistry
- Trypanosoma species research and implications
- Catalytic C–H Functionalization Methods
- Organic Light-Emitting Diodes Research
- Synthesis and Biological Evaluation
- Radical Photochemical Reactions
- Nanoplatforms for cancer theranostics
- Advanced Drug Delivery Systems
- Polysaccharides and Plant Cell Walls
- Chemical Reaction Mechanisms
- Sulfur Compounds in Biology
- Nanoparticles: synthesis and applications
- Research on Leishmaniasis Studies
- Dendrimers and Hyperbranched Polymers
- Carbon and Quantum Dots Applications
- Synthesis and Catalytic Reactions
- Nanoparticle-Based Drug Delivery
- Catalytic Cross-Coupling Reactions
- Innovative Microfluidic and Catalytic Techniques Innovation
- Cancer therapeutics and mechanisms
- Quinazolinone synthesis and applications
- Surfactants and Colloidal Systems
Universidade de Ribeirão Preto
2016-2024
Universidade de São Paulo
2015-2024
Clinics Hospital of Ribeirão Preto
2015
Neglected tropical diseases remain among the most critical public health concerns in Africa and South America. The drug treatments for these are limited, which invariably leads to fatal cases. Hence, there is an urgent need new antitrypanosomal drugs. To address this issue, a large number of diverse heterocyclic compounds were prepared. Straightforward synthetic approaches tolerated pre-functionalized structures, giving rise structurally set analogs. We report on 57 with selective activity...
Thiocyanation and formation of thioalkylated BODIPYs is a simple reliable way for their chemical modification photophysical tuning.
Abstract BODIPYs have a well‐established role in biological sciences as chemosensors and versatile markers due to their chemical reactivity, which allows for fine‐tuning of photophysical characteristics. In this work, we combined the unique reactivity arylazo sulfones with advantages “sunflow” reactor develop fast, efficient, method photochemical arylation other chromophores. This approach resulted red‐shifted emitting fluorophores extended electronic delocalization at 3‐ 5‐positions BODIPY...
The expansion of the fragment chemical space by accessing growth vectors two “heteroaromatic rings future” with regioselective functionalization is reported.
Abstract 4,4‐difluoro‐5,7‐dimethyl‐4‐bora‐3a,4a‐diaza‐s‐indacene (BODIPY) and derivatives are an outstanding class of fluorescent dyes. Herein, we report on the introduction a nitrosyl moiety into BODIPY structure its dramatic effect observed electrochemical reaction mechanism. 6‐Nitrosyl‐8‐phenyl‐BODIPY 5‐nitrosyl positional isomer, compounds 2 3 , respectively, were obtained from meso precursor, 8‐phenyl‐BODIPY ( 1 ), by nitrosation. Electrochemical studies for – reported. Cyclic...