Abstract
Alkylidenebis-2,2′-cyclohexanones react with two molecules of hydroxylamine to give 8-hydroxy-1,2,4,5-bistetramethylene-7-oxa-6,8-diazabicyclo[3.2.1]octanes, whereas 5,5′-methyl ene-2,2-dimethyl-4-pyrone and “semicyclic” and aliphatic-aromatic 1,5-diketones form dioximes.
Similar content being viewed by others
Literature cited
A. Palsky, J. Huet, and J. Dreux, Comptes Rend., C,262, 1543 (1966).
M. N. Tilichenko, Uch. Zap. Sarat. Gos. Univ.,75, 60 (1962).
G. Eikelmann, W. Heimberger, G. Nonnenmacher, and W. Weigert, Ann.,759, 183 (1972).
V. K. Gamov, T. V. Tropina, V. A. Kaminskii, and M. N. Tilichenko, Khim. Geterotsikl. Soedin., 1145 (1973).
J. Kondelikova, J. Kralicek, J. Smolikova, and K. Blaha, Coll. Czech. Chem. Commun.,38, 523 (1973).
V. I. Vysotskii, N. V. Vershinina, M. N. Tilichenko, V. V. Isakov, and T. M. Belokon', Zh. Organ. Khim.,9, 2427 (1973).
I. Wislicenus and R. Newmann, Ann.,302, 242 (1898).
Author information
Authors and Affiliations
Additional information
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1525–1526, November, 1974.
Rights and permissions
About this article
Cite this article
Gamov, V.K., Kaminskii, V.A. & Tilichenko, M.N. Structures of the products of reaction of 1,5-diketones with hydroxylamine. Chem Heterocycl Compd 10, 1340–1341 (1974). https://doi.org/10.1007/BF01175094
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF01175094