This research demonstrates a novel synthesis method for (2,2'-bi)pyridines, suggesting potential applications in organic chemistry.
An effective synthetic approach to (2,2'-bi)pyridines having a fragment of ((,)-9,10-dihydro-9,10-[1,2]benzenoanthracene-2-yl)amine ((tryptycene-2-yl)amine) in the alpha position via their 1,2,4-triazine precursors has been proposed; the synthesis was made as a result of the nucleophilic substitution of the cyano group at the C5 position of 3-(2-pyridyl)-1,2,4-triazines and the subsequent Bodger reaction with 2,5-norbornadiene.
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S.S. Potapova (2025) studied this question.
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