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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >A Modified Procedure for the Synthesis of 5-Amino-3-Arylisoxazoles and Their Reactions With Tetrasulfur Tetranitride Antimony(v) Chloride Complex (S_4N_4 centre dot SbCl_5):Novel Synthesis of 3-aRYL-1,2,5-Thiadiazole-4-Carboxamides
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A Modified Procedure for the Synthesis of 5-Amino-3-Arylisoxazoles and Their Reactions With Tetrasulfur Tetranitride Antimony(v) Chloride Complex (S_4N_4 centre dot SbCl_5):Novel Synthesis of 3-aRYL-1,2,5-Thiadiazole-4-Carboxamides

机译:5-氨基-3-Arylisoxazoles的合成方法及其与四硫四氯化锑(v)氯化物络合物(S_4N_4中心点SbCl_5)的反应:3-aRYL-1,2,5-Thiadiazole-4-的新颖合成羧酰胺

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摘要

Dropwise adition of #alpha3-bromo ketoximes ot a solution of KCN in MeOH at room temperature gave 5-amino-3-arylisoxazoles in moderate to good yields.Treatment of the isoxazoles prepared with tetrasulfur tetranitride antimony (V) chloride complex (S_4N_4 centre dot SbCl_5) in toluene at 100degC afforded novel 3-aryl-1,2,5-thiadiazole-4-carboxamides.
机译:室温下在KCN的MeOH溶液中滴加#alpha3-溴代酮肟,以中等至良好的产率得到5-氨基-3-芳基异恶唑。用四氮化四硫氯化锑(V)络合物制备的异恶唑的处理(S_4N_4中心点在100℃下在甲苯中的SbCl_5)得到新的3-芳基-1,2,5-噻二唑-4-羧酰胺。

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