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Synthesis of 3-Indole Substituted Sulfonyl 4H-Chromenes Using Recyclable Cyclometrix Polyphosphazene-Base Catalysts

机译:使用可回收的环甲甲磷酸聚磷酸基催化剂合成3个矿物取代的磺酰基4H-chromenes

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In order to build a library of 3-indole substituted sulfonyl 4H- chromenes in green protocol the three-component one-pot coupling reactions of substituted salicylaldehydes, sulfonyl acetonitriles and indoles have been performed using recyclable and metal-free heterogeneous base catalysts. The highly cross- linked cyclometrix polyphosphazenes (cPOPs) synthesized via a single-step precipitation polymerization of hexachlorocyclotri- phosphazene with 4,4’-oxydianiline or 3,3’-diaminobenzidine without using any other additives or surfactants were used as catalysts considering the resultant cPOPs intrinsically bear multiple amine moieties on their surface. The resultant cPOP microspheres showed excellent catalytic activity for variety of substrates at mild reaction conditions using a minimum amount of non-hazardous solvent. No laborious product work- up and purification procedures were needed and the cPOPs catalysts were recyclable up to six cycles without leeching and deactivation, satisfying green chemistry principles.
机译:为了在绿色方案中构建3个矿物替代的磺酰基4H-铬enens的库,使用了取代的水杨醛的三组分一锅偶联反应,使用磺酰基乙腈和吲哚进行了使用,并使用了无回收和无金属的异质基碱催化剂进行。高度交叉连接的环旋糖聚磷酸(CPOPS)是通过与4,4'-氧基二烯烯或3,3'-二氨基苯胺的单步降水聚合与六氯环磷酸的单步降水聚合,而无需使用任何其他添加剂或表面活性剂,而无需使用任何其他添加剂或表面表面。 CPOP在其表面上本质上带有多个胺部分。最终使用最少量的非危害溶剂,在轻度反应条件下,在轻度反应条件下各种底物显示出极好的催化活性。不需要艰苦的产品工作和纯化程序,CPOPS催化剂是可回收的最多六个周期的,而无需牵引和失活,从而满足了绿色化学原则。

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