Journal of Siberian Federal University. Chemistry / Preparation of Adamantyl and t-butyl Oximes Derivatives of 1,3- and 1,4-Dihydroxynaphthalene Diketone Tautomers

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Issue
Journal of Siberian Federal University. Chemistry. 2017 10 (3)
Authors
Peterson, Ivan V.; Svirskaya, Nadezhda M.; Kondrasenko, Alexander A.; Rubaylo, Anatoliy I.
Contact information
Peterson, Ivan V.: Institute of chemistry and chemical technology SB RAS FRC “Krasnoyarsk Science Center SB RAS”; 50/24 Akademgorodok, Krasnoyarsk, 660036, ; Svirskaya, Nadezhda M.: Institute of chemistry and chemical technology SB RAS FRC “Krasnoyarsk Science Center SB RAS”. 50/24 Akademgorodok, Krasnoyarsk, 660036, Russia; Kondrasenko, Alexander A.: Institute of chemistry and chemical technology SB RAS FRC “Krasnoyarsk Science Center SB RAS” 50/24 Akademgorodok, Krasnoyarsk, 660036, Russia; Rubaylo, Anatoliy I.: Siberian Federal University 79 Svobodny, Krasnoyarsk, 660041, Russia
Keywords
adamantane; oximation; diketone forms of dihydroxynaphthalenes
Abstract

Adamantyl and tert-butyl derivatives of 1,4-dihydroxynaphthalene diketone tautomer react with hydroxylamine in the pyridine and methanol medium with formation of corresponding monooximes. In the case of 1,3-dihydroxynaphthalene diketone tautomer only adamantylated oxime was synthesized

Pages
304-310
Paper at repository of SibFU
https://elib.sfu-kras.ru/handle/2311/68937