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This article is cited in 7 scientific papers (total in 7 papers)
Communications
2-Methyl-11-nitro-5,6-dihydro-2H-2,6-methano- 1,3,5-benzoxadiazocin-4(3H)-one: Synthesis, Crystal Structure and Tautomerism in Dipolar Aprotic Solvents
V. F. Sedova, V. P. Krivopalov, Yu. V. Gatilov, O. P. Shkurko
N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
Abstract:
Condensation of salicylaldehyde with nitroacetone and urea yields one diastereomer of the title compound. In DMF or DMSO solutions, this compound undergoes oxadiazocine ring opening leading to the equilibrium between its 2R*,6S*,11S*- and 2R*,6S*,11R*-diastereomers and 4-(2-hydroxyphenyl)-6-methyl-5-nitro-3,4-dihydropyrimidin-2(1H)-one.
Citation:
V. F. Sedova, V. P. Krivopalov, Yu. V. Gatilov, O. P. Shkurko, “2-Methyl-11-nitro-5,6-dihydro-2H-2,6-methano- 1,3,5-benzoxadiazocin-4(3H)-one: Synthesis, Crystal Structure and Tautomerism in Dipolar Aprotic Solvents”, Mendeleev Commun., 23:3 (2013), 176–178
Linking options:
https://www.mathnet.ru/eng/mendc2654 https://www.mathnet.ru/eng/mendc/v23/i3/p176
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