McMorn Paul, Hutchings Graham J
Department of Chemistry, Cardiff University, P.O. Box 912, Cardiff, UKCF10 3TB.
Chem Soc Rev. 2004 Feb 20;33(2):108-22. doi: 10.1039/b200387m. Epub 2004 Jan 29.
Enantioselective formation of C-H, C-C, C-O and C-N bonds has been extensively studied using homogeneous asymmetric catalysts for many years. However, these catalysts have yet to make a significant impact in the industrial synthesis of fine chemicals. A central reason is that homogeneous asymmetric catalyst design requires relatively bulky ligands and catalyst re-use through recovery and recycle often causes problems. One mechanism to overcome this problem is to immobilise the asymmetric catalyst onto a support and the resulting heterogeneous asymmetric catalyst can, in principle, be readily re-used. This tutorial review covers the different methodologies for immobilisation, including: adsorption, encapsulation, tethering using a covalent bond and electrostatic interaction and is aimed at both researchers new to the field and those with a wider interest in the immobilisation of homogeneous catalysts. Most importantly, recent studies will be highlighted that demonstrate that immobilised catalysts can give higher enantioselection when compared with their non-immobilised counterparts and the question of how high enantioselection can be achieved is addressed.
多年来,使用均相不对称催化剂对C-H、C-C、C-O和C-N键的对映选择性形成进行了广泛研究。然而,这些催化剂尚未在精细化学品的工业合成中产生重大影响。一个主要原因是均相不对称催化剂设计需要相对庞大的配体,并且通过回收和循环进行催化剂再利用常常会引发问题。克服这个问题的一种方法是将不对称催化剂固定在载体上,原则上,由此产生的多相不对称催化剂可以很容易地再利用。本教程综述涵盖了不同的固定方法,包括:吸附、包封、使用共价键和静电相互作用进行 tethering(文中该词未明确含义,可保留英文),目标受众是该领域的新手研究人员以及对均相催化剂固定化更感兴趣的人员。最重要的是,将重点介绍最近的研究,这些研究表明与未固定化的对应物相比,固定化催化剂可以给出更高的对映选择性,并探讨如何实现高对映选择性的问题。