Reactions of indolizines with cyclic ketones

被引:0
|
作者
Yurchenko, A.A. [1 ]
Kirzhner, I.A. [1 ]
Tolmachov, A.A. [1 ]
Pinchuk, A.M. [1 ]
机构
[1] Inst. Organicheskoj Khimii, NAN Ukrainy, Kiev, Ukraine
来源
Ukrainskij Khimicheskij Zhurnal | 2003年 / 68卷 / 11-12期
关键词
Acidity - Catalysis - Ketones - Nitrogen compounds - Nuclear magnetic resonance spectroscopy;
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摘要
The reaction of 2-substituted indolizines with an excess of cyclic ketone under acidic catalysis conditions was studied. It is established that the reaction products represent the corresponding 1,3-dicyclopentenyl-, cyclohexenyl-, and cycloheptenylindolizines. In the case of 2,3-disubstituted indolizines (for example, 3-aroyl-2-methylindolizine) the reaction proceeds at the position 1 of the heterocycle with the formation of 1-cyclopentenyl-, 1-cyclohexenyl-, and 1-cycloheptenyl-3-aroyl-2-methylindolizines. The data on NMR spectroscopy of the reaction products are given.
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页码:105 / 107
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