Abstract
The introduction of fluorine groups to pharmaceutical compounds can have a dramatic effect on the lipophilicity and metabolic stability of the molecule in vivo. Around 20 % of drugs contain at least one fluorine atom. The trifluoromethyl group is known to have beneficial effects and can dramatically affect the biological activity when substituted for a methyl group, for example. In any case, the direct and late-stage introduction of a trifluoromethyl group is a powerful transformation in the tool box of the medicinal chemist. The use of methyl fluorosulfonyldifluoroacetate (MFSDA) as a relatively inexpensive reagent for trifluoromethylation was first reported in 1989; however, in our opinion it has been somewhat underutilised. Herein, a comprehensive review of trifluoromethylation using MFSDA is reported, which we hope will further expose readers to this useful reagent.
| Original language | English |
|---|---|
| Pages (from-to) | 1219-1230 |
| Number of pages | 12 |
| Journal | Chemistry - A European Journal |
| Volume | 23 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 26 Jan 2017 |
Keywords
- fluorine
- methyl fluorosulfonyldifluoroacetate
- trifluoromethylation
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