Vinylamines, perfluoro

Electrochemical fluorination of cyclic 2-(dialkylamino)-propionic acids provides a general route to optically active perfluoro-(2-cycIic(dialkyl-amino)-propionic acids [91 JFC(52) 133], which are a source of perfluorinated vinylamines (88CL1887). 

An analogous reaction is the formation of perfluoro(l-vinylazepane) (14), perfluoro(l,4-divinylpiperazine) (15), and various perfluoro(vinylamines) 16. ... 

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See also in sourсe #XX -- [ , ]

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