循环醇的催化环扩张由质子合电子转移实现
Kuo Zhao1, Kenji Yamashita1, Joseph E Carpenter2
1Department of Chemistry , Princeton University , Princeton , New Jersey 08544 , United States.
Journal of the American Chemical Society
|May 24, 2019
概括
这项研究介绍了循环醇的催化环扩张方法. 该过程选择性地将N-成员环转化为N+1或N+2环添加物,使用基质中间体.
科学领域:
- 有机化学
- 催化剂
- 合成方法
背景情况:
- 循环亚利法醇是常见的结构图案.
- 在有机合成中,有效的环扩张方法是有价值的.
- 控制环扩张的区域选择性仍然是一个挑战.
研究的目的:
- 开发一种用于循环亚利法醇模块化环扩张的新型催化方法.
- 为了实现可控区域化学的选择性扩展产品的形成.
主要方法:
- 使用醇基质的质子合电子转移 (PCET) 激活.
- 产生用于C-C键裂变的基中间体.
- 使用基因重组与氨酸受体进行环扩张.
主要成果:
- 建立了循环亚利法醇环扩张的催化方法.
- 该方法通过基和基中间体进行.
- C-C 键形成的区域选择性由氨酸替代剂控制.
- 来自N个环的n+1和n+2环的选择性合成.
结论:
- 开发的催化方法提供了一个模块化的环扩张方法.
- 这种策略可以精确控制C-C键形成的区域选择性.
- 该方法可以选择性合成多种环膨胀.
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