Ikariya Takao, Murata Kunihiko, Noyori Ryoji
Department of Applied Chemistry, Graduate School of Science and Engineering, Tokyo Institute of Technology, 2-12-1 O-okayama, Meguro-ku, Tokyo, 152-8552, Japan.
Org Biomol Chem. 2006 Feb 7;4(3):393-406. doi: 10.1039/b513564h. Epub 2005 Dec 22.
The discovery and development of conceptually new chiral bifunctional transition metal-based catalysts for asymmetric reactions is described. The chiral bifunctional Ru catalyst was originally developed for asymmetric transfer hydrogenation of ketones and imines and is now successfully applicable to enantioselective C-C bond formation reaction with a wide scope and high practicability. The deprotonation of 1,3-dicarbonyl compounds with the chiral amido Ru complexes leading to the amine Ru complexes bearing C- or O-bonded enolates, followed by further reactions with electrophlies gives C-C bond formation products. The present bifunctional Ru catalyst offers a great opportunity to open up new fundamentals for stereoselective molecular transformation including enantioselective C-H and C-C as well as C-O, C-N bond formation.
本文描述了用于不对称反应的概念全新的手性双功能过渡金属基催化剂的发现与开发。手性双功能钌催化剂最初是为酮和亚胺的不对称转移氢化反应而开发的,如今已成功应用于对映选择性碳-碳键形成反应,具有广泛的适用范围和高实用性。手性酰胺基钌配合物使1,3-二羰基化合物去质子化,生成带有碳键或氧键烯醇盐的胺钌配合物,随后与亲电试剂进一步反应,得到碳-碳键形成产物。目前的双功能钌催化剂为开拓立体选择性分子转化的新基础提供了绝佳机会,包括对映选择性碳-氢和碳-碳以及碳-氧、碳-氮键的形成。