355137-26-7Relevant articles and documents
Reactivity of stable trifluoroacetaldehyde hemiaminals. 1. An unexpected reaction with enolizable carbonyl compounds
Blond,Billard,Langlois
, p. 4826 - 4830 (2001)
In the presence of enolizable carbonyl compounds, hemiaminals of fluoral and related polyfluoroaldehydes behave as equivalents of fluoroalkyl iminium compounds and provide β-polyfluoroalkyl β-dialkylamino ketones, which are easily transformed, under acidic conditions, into β-polyfluoroalkylenones.