P. Krasnikov, E. A. Sidnin, V. Osyanin
Oct 8, 2014
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Journal
Chemistry of Heterocyclic Compounds
Abstract
The interaction of nitrosochlorides based on 2-alkylidene adamantanes and 1Н-azoles in pyridine medium produced α-azolyl oximes of adamantane series. The reaction occurred as a conjugated 1,4-addition to in situ generated nitrosoalkenes acting as Michael acceptors. The structure of phenyl-[2-(4-phenyl-1Н-imidazol-1-yl)adamantan-2-yl]methanone (Е)-oxime was studied by X-ray crystallography.