首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >Regio-and stereoselective cycloadditions and further transformations of azomethine imine derivatives of fused [1,2,4]triazines
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Regio-and stereoselective cycloadditions and further transformations of azomethine imine derivatives of fused [1,2,4]triazines

机译:[1,2,4]三嗪稠合的区域和立体选择性环加成反应以及偶氮甲亚胺亚胺衍生物的进一步转化

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摘要

1,3-Dipolar cycloadditions of azomethine imine derivatives of dihydro[l,2,4]triazolo[3,4-c]benzo[l,2,4]triazines with asymmetric dienophiles proceeded in regio- and stereoselective manner.Cycloadditions with fumaronitrile resulted in a mixture of epimeric products,which under more forced conditions underwent ring opening reaction.Comparison of results obtained with cycloadditions with fumaric and maleic acid derivatives provided experimental support for the suggested epimerization.The dipolar cycloadditions were extended for isocyanates and isothiocyanates to yield new fused triazolinones and triazoline thiones.
机译:二氢[l,2,4]三唑并[3,4-c]苯并[l,2,4]三嗪的偶氮甲亚胺衍生物的1,3-偶极环加成反应与不对称亲二烯体反应以立体选择性和立体选择性方式进行。产生了差向异构体产物的混合物,该混合物在更强的条件下发生开环反应。与富马酸和马来酸衍生物的环加成反应的比较为建议的差向异构化提供了实验支持。偶极环加成反应扩展了异氰酸酯和异硫氰酸酯的生成稠合的三唑啉酮和三唑啉硫酮。

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