化环二甲 (III) 复合物可实现高度反选择性的3d-金属催化C-H功能化
Kristers Ozols1, Yun-Suk Jang1, Nicolai Cramer1
1Laboratory of Asymmetric Catalysis and Synthesis, Institute of Chemical Sciences and Engineering, École Polytechnique Fédérale de Lausanne (EPFL) , Lausanne CH-1015 , Switzerland.
新的 (III) 复合物与性配体使得高效的不对称C-H功能化成为可能. 这些催化剂在合成二异诺方面具有很高的反选择性,优于 (III) 方法.
科学领域:
- 有机金属化学
- 不对称的催化
- 合成有机化学
背景情况:
- 在金属催化反应中控制立体化学的重要作用.
- 非对称的C-H功能化是有效的分子合成的关键策略.
- 的催化提供了一个有前途的替代品,
研究的目的:
- 合成和表征具有三位置换的性环二烯联体的新型 (III) 复合物.
- 研究这些新的复合物的固体和电子性质.
- 评估它们在不对称的C-H功能化反应中的潜力.
主要方法:
- 合成 (III) 复合物与量身定制的奇拉环丁烯基连接物.
- 合成的复合物的静电和电子参数的详细映射.
- 在非对称的C-H功能化反应中使用复合物作为催化剂,特别是从N-胺和中合成二化.
主要成果:
- 一系列新的 (III) 复合物的成功合成和表征.
- 证明复合物在催化不对称的C-H功能化的有效性.
- 在二异诺合成中获得了优异的异选择性 (高达99. 5: 0. 5er) 和高区域选择性.
- 超越现有的基于的方法进行这种转化.
- 即使是具有挑战性的基质,如基,也表现出高的区域选择性和反选择性.
结论:
- 开发的 (III) 复合物是不对称的C-H功能化的高效催化剂.
- 这些复合物代表了这一反应类的 (III) 催化剂的显著进步.
- 该方法提供了一种可靠的选择性途径,以获得有价值的二化类产品.
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