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基于咪唑标记的双恶唑啉催化剂在不对称 Henry 反应中的催化作用和可回收性。

Catalytic effect and recyclability of imidazolium-tagged bis(oxazoline) based catalysts in asymmetric Henry reactions.

机构信息

R&D Centre for Pharmaceuticals, School of Chemical Engineering and the Environment, Beijing Institute of Technology, Beijing, PR China.

出版信息

Org Biomol Chem. 2012 Mar 14;10(10):2113-8. doi: 10.1039/c2ob06434k. Epub 2012 Jan 26.

Abstract

Functional imidazolium ionic liquids have been developed as a new class of versatile catalysts. C(2)-symmetric imidazolium-tagged bis(oxazoline) ligands were prepared, and the anions of the ligands were altered. The catalysts based on the new ligands and Cu(OAc)(2)·H(2)O were applied in asymmetric Henry reactions between various aldehydes 3 and CH(3)NO(2)4. The catalysts achieved a high level of enantioselectivity; product (R)-5n was attained at 94% ee in MeOH. Moreover, the catalyst could be recycled 6 times without an obvious loss of activity or enantioselectivity. In addition, a theoretical mechanistic study was conducted to explain the origin of the enantioselectivity.

摘要

功能化咪唑离子液体已被开发为一类新型多功能催化剂。我们制备了 C(2)对称的咪唑标记双恶唑啉配体,并改变了配体的阴离子。以新型配体和 Cu(OAc)(2)·H(2)O 为基础的催化剂应用于各种醛 3 和 CH(3)NO(2)4 之间的不对称 Henry 反应。这些催化剂实现了高的对映选择性;在甲醇中,产物 (R)-5n 的对映体过量值达到了 94%。此外,催化剂可以回收 6 次而没有明显的活性或对映选择性损失。此外,还进行了理论机理研究以解释对映选择性的起源。

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