R. I. Baichurin, A. V. Fel’gendler, L. V. Baichurina, S. V. Makarenko
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α-Nitrocinnamic Nitriles in Reactions with 1-Methylpyrrole, Hydrazine, Phenylhydrazine, and o-Aminothiophenol
The reaction of unsubstituted α-nitrocinnamic nitrile with 1-methylpyrrole ends with the formation of an AdN product, whereas the reactions of 2-aryl-2-nitroacrylonitriles with such N,N- and N,S-binucleophiles as hydrazine, phenylhydrazine, and o-aminothiophenol lead to transformation products of the initially formed adducts, linear azines and phenylhydrazones, or to a heterocyclic benzothiazole structure.
期刊介绍:
Russian Journal of General Chemistry is a journal that covers many problems that are of general interest to the whole community of chemists. The journal is the successor to Russia’s first chemical journal, Zhurnal Russkogo Khimicheskogo Obshchestva (Journal of the Russian Chemical Society ) founded in 1869 to cover all aspects of chemistry. Now the journal is focused on the interdisciplinary areas of chemistry (organometallics, organometalloids, organoinorganic complexes, mechanochemistry, nanochemistry, etc.), new achievements and long-term results in the field. The journal publishes reviews, current scientific papers, letters to the editor, and discussion papers.