Beilstein J. Org. Chem.2019,15, 1441–1447, doi:10.3762/bjoc.15.144
discovery chemistry. It is however, significantly less lipophilic than aryl-SCF3 which may offer a practical advantage in tuning overall pharmacokinetic profiles of molecules in development.
Keywords: Cunninghamella elegans; cytochrome P450; fluorinated substituents; organofluorinemetabolism
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Graphical Abstract
Figure 1:
Structures of trifluoromethyl sulfonyl ether bioactives.