整合金属催化C-H和C-O功能化,以实现化控制的区域选择性
Nicholas A Serratore1, Constance B Anderson1, Grant B Frost1
1Department of Chemistry , University of Minnesota-Twin Cities , 207 Pleasant Street SE , Minneapolis , Minnesota 55455 , United States.
Journal of the American Chemical Society
|July 11, 2018
概括
这项研究引入了一种新的催化反应,用于使用酸盐的区域选择性化. 这种方法实现了固态控制的C-C键形成,为合成有价值的芬衍生物提供了传统的电友芳香替代的替代方案.
科学领域:
- 有机金属化学
- 合成有机化学
- 催化剂
背景情况:
- 直接功能化C-H,C-C,C-O和C-N键是有机金属化学的一个关键目标.
- 通过Friedel-Crafts化进行电友芳香替代 (EAS) 是一种常见的烯基合成方法,但受到电子控制的区域选择性的限制.
- 实现与传统方法相反的反应选择性是一个重要的合成挑战.
研究的目的:
- 开发一种使用酸盐的固体控制的区域选择性酸盐化方法.
- 在各种化学物质中合成明显的替代,重要的结构动机.
- 探索一种新的反应机制,包括由催化的C-O和C-H激活.
主要方法:
- 催化直接与酸盐的化.
- 使用单个催化剂的C-O和C-H键激活的整合.
- 实验和计算研究以阐明反应机制.
主要成果:
- 通过硬质控制的区域选择合成.
- 一个独特的催化循环的演示,包括没有外部氧化剂或基的C-O和C-H激活.
- 对和成分的合成范围进行广泛的探索.
- 对抗癌症药物基斯坦的简要合成.
结论:
- 已经建立了一种新且高效的催化方法,用于硬质控制的区域选择性化.
- 反应通过一种独特的机制进行,包括协同作用的C-O和C-H激活.
- 这种方法为合成替代和相关化合物的传统EAS提供了有价值的替代品.
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