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首页> 外文期刊>Russian Journal of Organic Chemistry >Reactions of Ethyl 1-Benzyliclene-7a-hydroxy-4-phenyl-6-oxo-octahydro-1H-indene-5-carboxylate and Ethyl 5-Benzylidene-4a-hydroxy-1-pheeyl-3-oxodecahydronaphthalene-2-carboxylate with 2,2,4-Triazol-3-amine. Synthesis of Substituted Triazoloquinazolines
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Reactions of Ethyl 1-Benzyliclene-7a-hydroxy-4-phenyl-6-oxo-octahydro-1H-indene-5-carboxylate and Ethyl 5-Benzylidene-4a-hydroxy-1-pheeyl-3-oxodecahydronaphthalene-2-carboxylate with 2,2,4-Triazol-3-amine. Synthesis of Substituted Triazoloquinazolines

机译:1-苄基-7a-羟基-4-苯基-6-氧代-八氢-1H-茚基-5-羧酸乙酯与5-苄基-4a-羟基-1-苯基-3-氧代十二氢萘-2-羧酸乙酯的反应2,2,4-三唑-3-胺。取代的三唑并喹唑啉的合成

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摘要

Due to the presence of several reaction centers, hydroxy oxo derivatives of octahydroindene and deca-hydronaphthalene may be used as intermediate products in the synthesis of various complex systems. The 1,3-dicarbonyl fragment in their molecules is capable of being involved in heterocyclizations with difunc-tional nucleophiles. Reactions of such compounds with hydrazine and hydroxylamine were studied in sufficient detail [1]. However, only a few data are available on reactions of their analogs, hydroxyoxocyclo-hexanecarboxylates, with 3-amino-1,2,4-triazole [2]; the product structure was thoroughly studied using 2D NMR spectroscopy.
机译:由于存在多个反应中心,八氢茚和十氢化萘的羟基氧代衍生物可以用作合成各种复杂系统的中间产物。它们分子中的1,3-二羰基片段能够参与具有功能性亲核试剂的杂环化反应。充分详细地研究了此类化合物与肼和羟胺的反应[1]。然而,关于它们的类似物羟基氧代环己烷羧酸盐与3-氨基-1,2,4-三唑的反应,只有很少的数据[2]。使用2D NMR光谱对产品结构进行了深入研究。

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