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Defluorosilylation of trifluoromethane: upgrading an environmentally damaging fluorocarbon

Daniel J. Sheldon, Greg Coates, Mark R. Crimmin

2020Chemical Communications15 citationsDOIOpen Access PDF

Abstract

. The reaction generates a bench stable fluorinated building block that shows promise as an easy-to-use difluoromethylating agent. The difluoromethyl group is an increasingly important bioisostere in active pharmaceutical ingredients, and therefore our methodology creates value from waste. The potential scalability of the process has been demonstrated by achieving the reaction on a gram-scale.

Topics & Concepts

FluorocarbonChemical engineeringEnvironmentally friendlyChemistryMaterials scienceOrganic chemistryEngineeringEcologyBiologyFluorine in Organic ChemistryInorganic Fluorides and Related CompoundsPer- and polyfluoroalkyl substances research
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