Reactions of 2-aryl-4-arylidene-4H-oxazol-5-ones with 3-amino-1,2,4-triazole, 5-aminotetrazole, and 2-aminobenzimidazole

被引：0
作者：
V. A. Chebanov
S. M. Desenko
S. A. Kuzmenko
V. A. Borovskoy
V. I. Musatov
Yu. V. Sadchikova
机构：
[1] National Academy of Sciences of Ukraine,Scientific and Technological Corporation “Institute for Single Crystals”
来源：
Russian Chemical Bulletin | 2004年 / 53卷
关键词：
aminoazoles; 2-aryl-4-arylidene-4; -oxazol-5-ones; -[2-aryl-1-(azol-5-ylcarbamoyl)vinyl]aroylamides; -(7-aryl-5-oxo-4,5,6,7-tetrahydroazolo[1,5-; ]pyrimidin-6-yl)aroylamides; cyclocondensation; NMR spectroscopy;
D O I：
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学科分类号：
摘要：
The reactions of 3-amino-1,2,4-triazole, 5-aminotetrazole, and 2-aminobenzimidazole with 2-aryl-4-arylidene-4H-oxazol-5-ones (azlactones) were studied. The electron-releasing properties of the azole ring were demonstrated to influence the reaction pathway of azlactones with aminoazoles. The structures of the resulting compounds were established by 1H and 13C NMR spectroscopy using spin-spin decoupling and the nuclear Overhauser effect.
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页码：2845 / 2849
页数：4
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