Ring closure reactions O 0130 Cyanoethylation of Aromatic Aldehyde Imines Containing a Hydroxy Group in the βor γ-Position. Synthesis of 3-Cyanoethyl-1,3-oxazacycloalkanes. -(KON'KOVA, S. G.; ABOVYAN, G. M.; KHACHATRYAN, A. K.; BADASYAN, A. E.; PANOSYAN, G. A.; SARGSYAN, M. S.; Russ.
Acrylonitrile reacts with aromatic aldehyde imines containing a hydroxy group in the βor γposition to give 70-85% of the corresponding 2-aryl-3-cyanoethyltetrahydro-1,3-oxazines or 2-aryl-3-cyanoethyl-1,3-oxazolidines, respectively. The results of these reactions are rationalized in terms of ring-chain isomerism of the initial imines. n = 2, 3.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.