TRIFLU
Trifluoromethylation under Photoredox Catalysis
| Coordinatore | THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Organization address
address: University Offices, Wellington Square contact info |
| Nazionalità Coordinatore | United Kingdom [UK] |
| Totale costo | 231˙283 € |
| EC contributo | 231˙283 € |
| Programma | FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013) |
| Code Call | FP7-PEOPLE-2012-IIF |
| Funding Scheme | MC-IIF |
| Anno di inizio | 2013 |
| Periodo (anno-mese-giorno) | 2013-09-27 - 2015-09-26 |
Partecipanti
| # | ||||
|---|---|---|---|---|
| 1 |
THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Organization address
address: University Offices, Wellington Square contact info |
UK (OXFORD) | coordinator | 231˙283.20 |
Mappa
Word cloud
Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.
Obiettivo del progetto (Objective)
'Fluorine chemistry is critically important to advance a range of fields inclusive of medicinal chemistry, agrochemical chemistry as well as material science. In this context, there is a demand for new methods for the late stage selective trifluoromethylation of substrates that are not activated by the prototypical carbonyl group functionality. Such substrates require new catalytic manifolds to enhance reactivity and allow control over selectivity (regioselectivity, diastereoselectivity, chirality transfer, enantioselectivity). We propose to apply the concept of photoredox catalysis (visible light activation of transition metal complexes) for the trifluoromethylation of organosilanes and feedstock olefins.This study will include in depth understanding of reaction mechanisms (this will feature cyclic voltammetric measurements and electrochemistry) and will generate a library of compounds, the properties of which will be examined for potential application in drug discovery (GSK). The project will be carried out by an applicant who has expertise in fluorine chemistry and who is proficient in mechanistic studies. The host will bring complementary knowledge in fluorine chemistry, catalysis and photoredox catalysis. An ongoing external collaboration will add expertise in electrochemistry (Lyon). Upon completion, this project will contribute to advance catalysis in Europe and beyond and will allow the implementation of long lasting collaboration between Oxford and the Shanghai Institute of Organic Chemistry in China.'