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Exploring azide-enolate cycloaddition in the synthesis of novel Rufinamide analogs
Tetrahedron Letters ( IF 1.5 ) Pub Date : 2018-03-27 , DOI: 10.1016/j.tetlet.2018.03.075 José G. Aguirre-De Paz , Davir González-Calderón , Aydeé Fuentes-Benítes , Carlos González-Romero
中文翻译:
在合成新型Rufinamide类似物中探索叠氮化物-烯酸酯环加成反应
更新日期:2018-03-27
Tetrahedron Letters ( IF 1.5 ) Pub Date : 2018-03-27 , DOI: 10.1016/j.tetlet.2018.03.075 José G. Aguirre-De Paz , Davir González-Calderón , Aydeé Fuentes-Benítes , Carlos González-Romero
The exploration of azide-enolate cycloaddition in the synthesis of novel Rufinamide analogs is reported for the first time. A very simple procedure involving the use of β-ketonitriles as dipolarophiles afforded 5-aril/heteroayl Rufinamide derivatives in two steps.
中文翻译:
在合成新型Rufinamide类似物中探索叠氮化物-烯酸酯环加成反应
首次报道了在新型Rufinamide类似物的合成中对叠氮化物-烯酸酯环加成的探索。一个非常简单的程序,涉及使用β-乙腈作为双极性亲和剂,分两步提供了5-芳基/杂油基Rufinamide衍生物。