首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >MULTICOMPONENT SYNTHESIS OF NOVEL 2- AND 3-SUBSTITUTED DIHYDROBENZO[1,4]OXAZEPINONES AND TETRAHYDRO-BENZO[1,4]DIAZEPIN-5-ONES AND THEIR CONFORMATIONAL ANALYSIS
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MULTICOMPONENT SYNTHESIS OF NOVEL 2- AND 3-SUBSTITUTED DIHYDROBENZO[1,4]OXAZEPINONES AND TETRAHYDRO-BENZO[1,4]DIAZEPIN-5-ONES AND THEIR CONFORMATIONAL ANALYSIS

机译:新型2和3取代的双羟基苯并[1,4]恶二烯酮和四羟基苯并[1,4]二氮杂-5-酮的多组分合成及其结构分析

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摘要

By coupling an Ugi multicomponent condensation with a Mitsunobu reaction,a series of 2- and 3-substituted dihydrobenzo[l,4]oxazepinones and tetrahydrobenzo[l,4]diazepin-5-ones was synthesized in a very convergent manner.The strategy involves the use of substituted ethanolamines as amino components and of salicylic or N-methanesulphonyl anthranilic acid as carboxylic component.The general scope has been evaluated;in some cases better results have been obtained by reverting the order of the two reactions.A thorough conformational analysis on these products has been carried out through NMR,showing that in most cases a single conformation was strongly favoured.
机译:通过将Ugi多组分缩合反应与Mitsunobu反应偶联,以非常收敛的方式合成了一系列2-和3-取代的二氢苯并[1,4]氧杂a酮和四氢苯并[1,4]二氮杂-5-酮。使用取代的乙醇胺作为氨基组分,水杨酸或N-甲磺酰基邻氨基苯甲酸作为羧酸组分。已评估了一般范围;在某些情况下,通过还原两个反应的顺序获得了更好的结果。这些产物已经通过NMR进行了分析,表明在大多数情况下,强烈支持单一构象。

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