An efficient and selective approach for the synthesis of polyfunctionalised 3-fluoropyrroles has been developed starting from commercial aldehydes. The methodology is concise, efficient and allows for the modular and systematic assembly of polysubstituted 3-fluoropyrroles. This synthesis provides an alternative and highly convergent strategy for the generation of these chemically and biologically important units
Conselho Nacional de Desenvolvimento Científico e TecnológicoThis work presents a new, simple and ve...
Current approaches to drug discovery tends to involve the rapid analogue synthesis and testing of sm...
Synthesis of highly substituted 3-fluorofurans is reported. The sequence began with preparation of t...
Fluorinated compounds make up a large proportion of the output from both the pharmaceutical and agro...
Dans une première partie, une méthode efficace et générale de préparation de pyrroles E-fluoroalkylé...
Fluorination of a range of pyrrole substrates bearing various electron donating and withdrawing subs...
Fluorinated heterocyclic motifs have found wide application across the life science industries. Ther...
In a first part, an efficient and versatile method of preparation of E-fluoroalkylated pyrroles has ...
Per- and polyfluoroarenes are important synthetic chemistry targets because they are active componen...
Sequential reaction cascades for the synthesis of polysubstituted 2‐ and 3‐fluoropyrrole derivatives...
5-Alkoxymethyl-2-aryl-3-fluoro-1H-pyrroles and 2-aryl-3-fluoro-1H-pyrrole-5-carbaldehydes were effic...
Polyfunctional pyrroles are interesting heterocyclic intermediates as they have a range of reactive ...
During this 3-year PhD project in collaboration with Bayer CropScience, a family of fluorinating rea...
The project was divided into three parts: 1. Synthesis of perfluoro (highly fluorinated chain) ...
Organofluorine chemistry has played a significant role in the majority of the spectacular scientific...
Conselho Nacional de Desenvolvimento Científico e TecnológicoThis work presents a new, simple and ve...
Current approaches to drug discovery tends to involve the rapid analogue synthesis and testing of sm...
Synthesis of highly substituted 3-fluorofurans is reported. The sequence began with preparation of t...
Fluorinated compounds make up a large proportion of the output from both the pharmaceutical and agro...
Dans une première partie, une méthode efficace et générale de préparation de pyrroles E-fluoroalkylé...
Fluorination of a range of pyrrole substrates bearing various electron donating and withdrawing subs...
Fluorinated heterocyclic motifs have found wide application across the life science industries. Ther...
In a first part, an efficient and versatile method of preparation of E-fluoroalkylated pyrroles has ...
Per- and polyfluoroarenes are important synthetic chemistry targets because they are active componen...
Sequential reaction cascades for the synthesis of polysubstituted 2‐ and 3‐fluoropyrrole derivatives...
5-Alkoxymethyl-2-aryl-3-fluoro-1H-pyrroles and 2-aryl-3-fluoro-1H-pyrrole-5-carbaldehydes were effic...
Polyfunctional pyrroles are interesting heterocyclic intermediates as they have a range of reactive ...
During this 3-year PhD project in collaboration with Bayer CropScience, a family of fluorinating rea...
The project was divided into three parts: 1. Synthesis of perfluoro (highly fluorinated chain) ...
Organofluorine chemistry has played a significant role in the majority of the spectacular scientific...
Conselho Nacional de Desenvolvimento Científico e TecnológicoThis work presents a new, simple and ve...
Current approaches to drug discovery tends to involve the rapid analogue synthesis and testing of sm...
Synthesis of highly substituted 3-fluorofurans is reported. The sequence began with preparation of t...