...
首页> 外文期刊>Angewandte Chemie >Fragment Coupling Reactions in Total Synthesis That Form Carbon-Carbon Bonds via Carbanionic or Free Radical Intermediates
【24h】

Fragment Coupling Reactions in Total Synthesis That Form Carbon-Carbon Bonds via Carbanionic or Free Radical Intermediates

机译:整个合成中的片段偶联反应,可通过碳酸或自由基中间体形成碳 - 碳键

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Fragment coupling reactions that form carbon-carbon bonds are valuable transformations in synthetic design. Advances in metal-catalyzed cross-coupling reactions in the early 2000s brought a high level of predictability and reliability to carbon-carbon bond constructions involving the union of unsaturated fragments. By comparison, recent years have witnessed an increase in fragment couplings proceeding via carbanionic and open-shell (free radical) intermediates. The latter has been driven by advances in methods to generate and utilize carbon-centered radicals under mild conditions. In this Review, we survey a selection of recent syntheses that have implemented carbanion- or radical-based fragment couplings to form carbon-carbon bonds. We aim to highlight the strategic value of these disconnections in their respective settings and to identify extensible lessons from each example that might be instructive to students.
机译:形成碳-碳键的片段偶联反应是合成设计中有价值的转换。21世纪初,金属催化的交叉偶联反应的进展为涉及不饱和片段结合的碳-碳键结构带来了高度的可预测性和可靠性。相比之下,近年来,通过碳阴离子和开壳(自由基)中间体进行的片段偶联增加。后者是由温和条件下产生和利用碳中心自由基的方法的进步推动的。在这篇综述中,我们回顾了一些最近的合成,这些合成已经实现了基于碳负离子或自由基的片段偶联以形成碳-碳键。我们旨在强调这些断开在各自环境中的战略价值,并从每个示例中找出可能对学生有指导意义的可扩展课程。

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