Abstract
A method was developed for the synthesis of N-substituted 2,2,6,6-tetramethyl- and 1,2,-2.6,6-pentamethyl-4-aminopiperidines starting from triacetoneamine cyanohydrin through the corresponding aminonitriles with subsequent reductive decyanation. The peculiarities of salt formation from N-substituted 4-aminopiperidines with a shielded nitrogen atom are examined.
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