Antiviral activity of adamantane series hydroxy derivatives
作者:Yu. N. Klimochkin、M. V. Leonova、I. R. Korzhev、I. K. Moiseev、G. V. Vladyko、L. V. Korobchenko、E. I. Boreko、S. N. Nikolaeva
DOI:10.1007/bf00777145
日期:1992.7
Previous authors [i] have established the fact that introducing hydroxyl groups into the adamantane framework broadens the scope of antiviralactivity as well as reduces toxicity. For example, 3,5-dimethyl-7-ethyladamantanol-i exhibits pronounced activity with respect to herpes, influenza and vaccine viruses [2]. It might be expected that changing the lipophilic capacity of the skeletal fragment when
Moiseev, I. K.; Doroshenko, R. I., Journal of Organic Chemistry USSR (English Translation), 1983, p. 999
作者:Moiseev, I. K.、Doroshenko, R. I.
DOI:——
日期:——
Selective Nitroxylation of Adamantane Derivatives in the System Nitric Acid–Acetic Anhydride
作者:Yu. N. Klimochkin、E. A. Ivleva、I. K. Moiseev
DOI:10.1134/s1070428020090055
日期:2020.9
A number of new nitroxyadamantanes have been synthesized by nitroxylation of the corresponding substrates with nitric acid in acetic anhydride. High electrophilicity and reduced acidity of the system HNO3-Ac2O increases the stability of nitrates and significantly decreases the probability of formation of alcohols. In some cases, nitrolysis and oxidation of functional groups in the substrate are observed.
Moiseev, I. K.; Doroshenko, R. I., Journal of Organic Chemistry USSR (English Translation), 1982, p. 1067 - 1069
作者:Moiseev, I. K.、Doroshenko, R. I.
DOI:——
日期:——
Moiseev, I. K.; Stulin, N. V.; Yudashkin, A. V., Journal of general chemistry of the USSR, 1985, vol. 55, # 7, p. 1472 - 1473
作者:Moiseev, I. K.、Stulin, N. V.、Yudashkin, A. V.、Klimochkin, Yu. N.