...
首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Toward a novel approach to bis-β-lactam synthesis using Vilsmeier reagent as an efficient entity via Staudinger cycloaddition reaction
【24h】

Toward a novel approach to bis-β-lactam synthesis using Vilsmeier reagent as an efficient entity via Staudinger cycloaddition reaction

机译:迈向一种新的方法,利用Vilsmeier试剂作为有效实体,通过Staudinger环加成反应合成双-β-内酰胺

获取原文
获取原文并翻译 | 示例
           

摘要

A facile synthesis of bis-β-lactams has been executed using chloromethylenedimethylammonium chloride (Vilsmeier reagent), prepared easily from N,N-dimethylformamide and phosphorus oxychloride. It works out as a versatile acid activator reagent for the direct [2 + 2] ketene-imine cycloaddition of substituted acetic acid and bis-imines in one-pot synthesis under mild conditions. Thus, this method has been proved as a high yielding, efficient, and cheap protocol for bis-β-lactam synthesis.
机译:已经使用氯亚甲基二甲基氯化铵(Vilsmeier试剂)轻松进行了双-β-内酰胺的合成,该反应可由N,N-二甲基甲酰胺和三氯氧化磷轻松制得。它是一种通用的酸活化剂,可在温和条件下通过一锅法直接将[2 + 2]烯酮-亚胺基环加成取代的乙酸和双亚胺。因此,已证明该方法是双-β-内酰胺合成的高产率,有效且廉价的方案。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号