通过对氨基cyclopropanes的定向C-C键激活对Azepines的模块化访问
1School of Chemistry, University of Bristol , Bristol, BS8 1TS, United Kingdom.
Journal of the American Chemical Society
|February 21, 2018
概括
这项研究提出了一种新型催化方法来合成阿泽. 该过程使用C-C键激活和C-H功能化进行高效,无副产品的异环化.
科学领域:
- 有机化学
- 催化剂
- 异环化学
背景情况:
- 阿泽是重要的含异环,具有多种应用.
- 开发高效的模块化合成途径仍然是有机合成的关键挑战.
研究的目的:
- 开发一种新的模块化催化方法,用于合成阿齐环系统.
- 使用C-C键激活和C-H功能化进行高效的异环化.
主要方法:
- 在一氧化碳 (CO) 大气下使用催化剂.
- 使用保护组指向氨基cyclopropanes的C-C键激活以形成rhodacyclopentanone中间体.
- 进行N-aryl或N-vinyl单元的分子内C-H化.
主要成果:
- 罗达cyclopentanone中间体的成功合成.
- 这些中间体在分子内C-H化中的有效性已被证明.
- 通过顺序的C-C激活和C-H功能化实现无副产品的异环化.
结论:
- 已经建立了一个模块化和高效的催化策略来合成阿泽.
- 该方法依赖于C-C键激活和C-H功能化的序列.
- 这种方法为阿西脚架提供了一条有价值的新途径.
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