Abstract:Gold-catalyzed regioselective hydrofluorination of alkynes
using
aqueous HF has been achieved by employing an amide directing group.
For both aryl- and alkyl-substituted propargylamines, the fluorination
occurred at the site distal to the amino group.
The gold-catalyzed hydrofluorination of terminal alkynes is reported. The salient features of this study showcase the use of potassium bifluoride, KHF2, as the fluorinating agent in conjunction with a fluorinated...
Since the beginning of this century, there has been a great deal of research on homogeneous gold-catalyzed alkyne fluorination due to the precious values of fluorinated scaffolds in many bioactive...
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