Abstract
A first general approach to the synthesis of unsymmetri- cally substituted tris(b-oximinoalkyl)amines containing two or three different b-oximinoalkyl fragments has been developed. This procedure employs available aliphatic nitro compounds as starting building blocks and their silylation as the key step. This approach provides an efficient strategy for the diversity-oriented synthesis of 1,4,6,10-tetraazaadamantane derivatives.
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