首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Substituted 4-Oxo-1,2,3,4-tetrahydroquinoline-3-carboxylic esters by a tandem imine addition-S_NAr reaction
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Substituted 4-Oxo-1,2,3,4-tetrahydroquinoline-3-carboxylic esters by a tandem imine addition-S_NAr reaction

机译:通过串联亚胺加成-S_NAr反应取代4-氧-1,2,3,4-四氢喹啉-3-羧酸酯

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摘要

A tandem imine addition-S_NAr annulation reaction has been developed as a new approach to the synthesis of 4-oxo-1,2,3,4- tetrahydroquinoline-3-carboxylic esters. A series of these structures has been generated by reacting selected imines with tert-butyl 2-fluoro-5- nitrobenzoylacetate. Structural variations in the final products are accomplished by changing the substituents on the imine and the alkyl group of the ester. The title compounds are isolated as their enols in 55-97% yield without the need for added base or catalysts. The synthesis of the starting materials as well as mechanistic studies and further synthetic conversions of the products are presented.
机译:已经开发了串联亚胺加成-S_NAr环化反应,作为合成4-oxo-1,2,3,4-四氢喹啉-3-羧酸酯的新方法。通过使选定的亚胺与2-氟-5-硝基苯甲酰乙酸叔丁酯反应,已经产生了一系列这些结构。最终产物的结构变化是通过改变酯的亚胺和烷基上的取代基来实现的。以55-97%的收率分离标题化合物作为其烯醇,无需添加碱或催化剂。介绍了原料的合成以及产品的机理研究和进一步的合成转化。

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