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Selective Electrochemical Nucleophilic Fluorination

Project description

New Fluorination pathways to improve pharmaceuticals and medical imaging

Strategically placing fluorine atoms in organic compounds can significantly alter their properties. Fluorinated molecules improve pharmaceuticals and agrochemicals and act as radiotracers in high-resolution medical imaging technologies, such as positron emission tomography. While nucleophilic fluoride (F-) sources are cheap and readily available, their reactivity is less controllable and useful than that of electrophilic fluorine F+ sources. The EU-funded SENF project is working on a concept that could revolutionise fluorination chemistry, effectively transmuting F- into F+ to expand the range of useful chemical reactions. The ultimate aim is to create new pathways to more potent bioactive molecules for use in pharmaceuticals and medical imaging technologies.

Objective

The incorporation of fluorine into organic compounds is extremely important for designing molecules with specific function. Fluorine is primed for improving the pharmacokinetic properties of drugs and agrochemicals, and is crucial for the life-changing imaging technique, Positron Emission Tomography (PET). Thus, selective fluorination is an area of significant interest in organic synthesis.

This research programme will develop a concept that promises to revolutionise fluorination chemistry. While nucleophilic fluoride (F-) sources are inexpensive and readily available, they have unfavourable reactivity compared to electrophilic fluorine sources (F+), which are typically expensive, wasteful and not suited to either large scale synthesis or PET. By transmuting F- into F+, we can get the best of both worlds! We will develop a concept based on umpolung (polarity reversal) to invent a number of novel synthetic methodologies or to expand useful reactions into new chemical space. The overall vision is to create new pathways to new bioactive molecules that are either more potent, have improved pharmacokinetics, or can be new radiochemical tracers.

Our strategy relies on the combination of catalysis and electrochemical oxidation to perform this thermodynamically demanding task. The use of electrochemistry is essential for this strategy, because it is necessary to be able to dial-in any oxidising potential with high control. New organo- and organometallic catalysts, heterogeneous electrocatalysts and fluoride sources will be developed as part of the studies, which will be of value to the fields of fluorination, homogeneous catalysis, synthesis and energy research. Medicinal, process and radio chemists will all benefit as their toolbox of methods will expand, thereby facilitating the discovery and manufacture of drugs and chemicals that improve the quality of human life around the globe.

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Topic(s)

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ERC-STG - Starting Grant

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Call for proposal

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(opens in new window) ERC-2020-STG

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Host institution

UNIVERSITY OF BRISTOL
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 1 553 043,00
Address
BEACON HOUSE QUEENS ROAD
BS8 1QU BRISTOL
United Kingdom

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Region
South West (England) Gloucestershire, Wiltshire and Bristol/Bath area Bristol, City of
Activity type
Higher or Secondary Education Establishments
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Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

€ 1 553 043,00

Beneficiaries (1)

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