首页> 外文期刊>Chemistry of heterocyclic compounds >Recyclization of 1,3,4-Oxadiazoles and Bis-1,3,4-oxadiazoles into 1,2,4-Triazole Derivatives. Synthesis of 5-Unsubstituted 1,2,4-Triazoles
【24h】

Recyclization of 1,3,4-Oxadiazoles and Bis-1,3,4-oxadiazoles into 1,2,4-Triazole Derivatives. Synthesis of 5-Unsubstituted 1,2,4-Triazoles

机译:将1,3,4-恶二唑和Bis-1,3,4-恶二唑环化为1,2,4-三唑衍生物。 5-未取代的1,2,4-三唑的合成

获取原文
获取原文并翻译 | 示例
           

摘要

Efficient methods have been developed for obtaining precursors of stable carbenes, viz. 5-unsubstituted 3,4-diaryl-1,2,4-triazoles and 3,3′- or 4,4′-bridge linked bis-1,2,4-triazoles, by the recyclization of 5-unsubstituted 1,3,4-oxadiazoles or p-phenylenebis-1,3,4-oxadiazole with anilines or aromatic diamines in the presence of trifluoroacetic acid or with aniline hydrochlorides in pyridine.
机译:已经开发出用于获得稳定的卡宾的前体的有效方法。通过将5个未取代的1,3,3环化,将5个未取代的3,4-二芳基-1,2,4-三唑和3,3'-或4,4'桥连接的双-1,2,4-三唑在三氟乙酸存在下,或与苯胺盐酸盐在吡啶中,将4-4-恶二唑或对亚苯基-1,3,4-恶二唑与苯胺或芳族二胺一起使用。

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