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REACTIONS OF α-CHLORO- AND α,α-DICHLORO-β-CARBONYL-SUBSTITUTED ALDEHYDES WITH AMINES
Guseinov, F. I.,Klimentova, G. Yu.,Moskva, V. V.
, p. 530 - 533 (2007/10/02)
Depending on the nature of the substrate (the chlorodicarbonyl compound) and the nature of the nucleophilic reagent (the amine), the reaction of α-chloro- and α,α-dichloro-β-carbonyl-substituted aldehydes with amines takes place mainly in three directions i.e., with the formation of enamines or imines or with cleavage of the C-CHO bond of the aldehydes.
