...
首页> 外文期刊>Angewandte Chemie >Breaking Aromaticity with Aminocatalysis: A Convenient Strategy for Asymmetric Synthesis
【24h】

Breaking Aromaticity with Aminocatalysis: A Convenient Strategy for Asymmetric Synthesis

机译:用氨基酸分析破坏芳香性:非对称合成的方便策略

获取原文
获取原文并翻译 | 示例
           

摘要

Since the turn of the millennium, catalytic reactions promoted by primary or secondary amines have emerged as a highly useful method for organic chemistry. Very recently, the potential of such synthetic strategies has been vastly expanded by incorporating the principle of aromaticity breaking. Novel reaction pathways can now be accessed through the intermediacy of polyenamine intermediates derived from (hetero)aromatic systems. The proper design of carbonyl starting materials, combined with the high stereochemical efficiency provided by well-established aminocatalysts, has enabled the synthesis of products with (hetero)aromatic frameworks in highly enantio- and diastereomerically enriched form. In this Minireview, we provide an overview of recent advances in this field of research and familiarize the reader with new synthetic opportunities offered by these interesting methodologies.
机译:自千年之后,初级或仲胺促进的催化反应作为有机化学的高度有用的方法。 最近,通过纳入芳香性破碎原理,这种合成策略的潜力已经大大扩展。 现在可以通过衍生自(杂)芳族体系的多聚环胺中间体的中间体进入新的反应途径。 羰基原料的适当设计,结合良好的氨基催化剂提供的高立体化学效率,使得在高肾上腺和非映异构体富集的形式中能够合成(异质)芳族框架。 在这个MINIREVIEW中,我们概述了该研究领域的最新进展情况,并熟悉这些有趣方法提供的新的合成机会。

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