首页> 外文期刊>Journal of the American Chemical Society >A Strategy for C-H Activation of Pyridines: Direct C-2 Selective Aikenylation of Pyridines by Nickel/Lewis Acid Catalysis
【24h】

A Strategy for C-H Activation of Pyridines: Direct C-2 Selective Aikenylation of Pyridines by Nickel/Lewis Acid Catalysis

机译:吡啶的C-H活化策略:镍/路易斯酸催化的吡啶直接C-2选择性烯基化

获取原文
获取原文并翻译 | 示例
       

摘要

A large number of Pharmaceuticals, natural products, and optical materials contain a pyridine nucleus. Thus, the functionalization of pyridines is an important transformation in organic synthesis. However, due to the low reactivity of pyridine derivatives toward aromatic electrophilic substitution reactions such as the Friedel-Crafts reaction, additional steps including halogenation and meta- lation are required to install substituents in a pyridine ring.
机译:大量药品,天然产品和光学材料包含吡啶核。因此,吡啶的功能化是有机合成中的重要转变。但是,由于吡啶衍生物对芳族亲电取代反应(如Friedel-Crafts反应)的反应性低,需要其他步骤(包括卤化和间位反应)将取代基安装在吡啶环中。

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