为什么BINOL基单酸盐在Rh催化不对称的烯化中是如此有效的配体?
Manfred T Reetz1, Andreas Meiswinkel, Gerlinde Mehler
1Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, D-45470 Mülheim/Ruhr, Germany. reetz@mpi-muelheim.mpg.de
Journal of the American Chemical Society
|July 21, 2005
概括
这项研究揭示了化酸连接物如何在催化酸化过程中产生高反选择性. 一个锁钥匙机制,与经典方法不同,决定了立体化学结果.
科学领域:
- 有机金属化学 有机金属化学
- 不对称的催化剂.
- 机械学研究 机械学研究
背景情况:
- 使用BINOL衍生的单酸酸盐的化提供了一种高效的合成途径.
- 经常观察到高的酶选择性 (90-99% ee),但基本机制仍然不太清楚.
研究的目的:
- 阐明Rh催化烯与单酸酸盐化中的高反选择性背后的机制.
- 研究结合体协调和中间形成在立体化学控制中的作用.
主要方法:
- 核磁共振 (NMR) 光谱用于预催化剂的表征.
- 动力学研究,包括对非线性效应的分析.
- 密度函数理论 (DFT) 计算以建模反应路径.
主要成果:
- 鉴定证实了两个单酸酸盐连接物与的附着.
- 动力学和DFT研究支持了"锁与钥匙"机制.
- -烯复合的热力学通过二聚体中间体确定了立体化学结果.
结论:
- "锁与钥匙"机制由二聚体中间体形成驱动,解释了高的反反选择性.
- 这种机制与在传统的Rh催化化中观察到的"反锁与钥匙"机制形成鲜明对比.
相关概念视频
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