使用可调节的配体允许分子间Pd催化C-O键的形成
Andrei V Vorogushin1, Xiaohua Huang, Stephen L Buchwald
1Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Journal of the American Chemical Society
|June 2, 2005
概括
大量的二甲基酸连接物使得高效的催化C-O合反应. 这种方法首次成功将烯化物与各种酒精 (包括醇) 结合在一起.
科学领域:
- 有机化学 有机化学
- 催化剂是一种催化剂.
- 有机金属化学 有机金属化学
背景情况:
- 催化C-O合反应对于形成乙烯键至关重要.
- 传统的方法经常与未激活的烯化物和无菌阻碍的酒精作斗争.
- 消除β-化物可能是竞争性的副作用反应,限制了效率.
研究的目的:
- 为增强催化C-O合开发庞大的二甲基酸配体.
- 为了在C-O合反应中促进减小消除比β-化物消除.
- 为了实现未激活的化和初级和二级酒精的有效合.
主要方法:
- 在催化C-O合反应中利用了重的二甲基酸连接体.
- 系统地改变了连接体大小,以匹配基质的硬质性质.
- 使用的化和化与循环和非循环二次醇.
主要成果:
- 证明了重的二甲基酸连接物促进了减少性消除.
- 实现了未激活的化和化与二次醇的高效C-O合.
- 首次在催化过程中成功合醇.
结论:
- 大量的二甲基酸连接物对Pd催化C-O合有效.
- 质体大小匹配对于促进所需的还原性消除至关重要.
- 这种方法扩大了C-O合的范围,包括具有挑战性的基质,如醇.
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