在o-carboranes中的B-H键的区域选择性核性化/化:选择性子功能化的替代方法
Cen Tang1, Jiji Zhang1, Jie Zhang1
1Department of Chemistry and State Key Laboratory of Synthetic Chemistry , The Chinese University of Hong Kong , Shatin , New Territories, Hong Kong , China.
Journal of the American Chemical Society
|November 17, 2018
概括
一种新介导的方法使B-H键在o-carboranes中的区域选择性核友取代成为可能. 这种方法为合成选择性化和化O-碳酸提供了一种补充策略.
科学领域:
- 有机金属化学
- 化学
- 有机合成
背景情况:
- o-碳酸是具有独特电子特性的多功能集群.
- 目前用于功能化o-carboranes的方法包括过渡金属催化和电友替代.
- 开发区域选择性核替代方案对于扩大它们的合成效用至关重要.
研究的目的:
- 在o-carboranes中引入区域选择性核友B-H替代的新协议.
- 为了补充现有的过渡金属催化和电友替代策略.
- 合成新的B3,6-二甲基化和B9,6-基化/基化o-碳酸.
主要方法:
- 使用介导反应进行选择性核友取代.
- 反应的目标是O-碳酸的B(3,6) -H和B(9) -H位置.
- 对子C替代物的立体和电子因子进行了分析,以确定它们在选择性中的作用.
主要成果:
- 成功开发了一种区域选择性核友B-H替代的新方案.
- 获得了高基基和基基基基基基基基基.
- 发现C替代剂的固体和电子因素对位点选择性有显著的影响.
结论:
- 拟议的介导方法为o-carborane功能化提供了一种强大且互补的方法.
- 这一协议使得特定替代的o-carboranes的高效合成成为可能.
- 了解C替代剂的作用是控制核友替代反应中的区域选择性的关键.
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