首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Convenient method for the synthesis of macrocyclic teteraamides, acyclic diamides, their lariat derivatives and bis-macrocyclic tetraamides
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Convenient method for the synthesis of macrocyclic teteraamides, acyclic diamides, their lariat derivatives and bis-macrocyclic tetraamides

机译:合成大环叔胺,无环二酰胺,其套索衍生物和双大环四酰胺的简便方法

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摘要

The macrocyclic tetraamides 8a-e were obtained in good yields by bis-alkylation of the potassium salts of the appropriate bis-phenols 7a-c with the dihalo compounds 2a,b. Similarly, macrocyclic tetraamides with pendant hydroxy group 18a,b were prepared by the nucleophilic reaction of the potassium salts of 7a,b with the dihalo compound 10. Acylation of 18a,b with chloroacetyl chloride gave the corresponding ester 19a,b. Compounds 19a,b reacted with different secondary amines to afford the corresponding lariat macrocycles 20a-d and novel bis-macrocycle 21 in 50-65% yield. [References: 40]
机译:通过将合适的双酚7a-c的钾盐与二卤代化合物2a,b双烷基化,以高收率获得大环四酰胺8a-e。类似地,通过7a,b的钾盐与二卤代化合物10的亲核反应制备具有侧链羟基18a,b的大环四酰胺。18a,b与氯乙酰氯酰化,得到相应的酯19a,b。化合物19a,b与不同的仲胺反应,以50-65%的产率提供相应的套索状大环化合物20a-d和新型双-大环化合物21。 [参考:40]

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