Recent Advances in Ru Catalyzed Transfer Hydrogenation and Its Future Perspectives

N. Tyagi, Gongutri Borah, Pitambar Patel, D. Ramaiah
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引用次数: 2

Abstract

Over the past few decades, Ru catalyzed transfer hydrogenation (TH) and asymmetric transfer hydrogenation (ATH) reactions of unsaturated hydrocarbons, imine, nitro and carbonyl compounds have emerged as economic and powerful tools in organic synthesis. These reactions are most preferred processes having applications in the synthesis of fine chemicals to pharmaceuticals due to safe handling as these do not require hazardous pressurized H2 gas. The catalytic activity and selectivity of Ru complexes were investigated with a variety of ligands based on pincer NHC, cyclophane, half-sandwich, organophosphine etc. These ligands coordinate to Ru center in a proper orientation with a labile group replaced by H-source (like methanol, isopropanol, formic acid, dioxane, THF), which facilitate the β-hydrogen transfer to generate metal hydride species (Ru-H) and produce desired reduced product. This chapter describes the recent advances in TH and ATH reactions with homogeneous and heterogeneous Ru catalysts having different ligand environments and mechanistic details leading to their sustainable industrial applications.
钌催化转移加氢研究进展及展望
在过去的几十年里,钌催化不饱和烃、亚胺、硝基和羰基化合物的转移加氢(TH)和不对称转移加氢(ATH)反应成为有机合成中经济而有力的工具。由于不需要危险的加压氢气,这些反应在精细化学品到药物的合成中具有安全的处理,因此是最优选的过程。采用钳形NHC、环烷、半夹心、有机膦等配体研究了钌配合物的催化活性和选择性。这些配体以合适的方向与Ru中心配位,用h源(如甲醇、异丙醇、甲酸、二恶烷、四氢呋喃)取代不稳定基团,促进β-氢转移生成金属氢化物(Ru- h),生成所需的还原产物。本章描述了使用具有不同配体环境和机理细节的均相和非均相Ru催化剂进行TH和ATH反应的最新进展,从而导致其可持续的工业应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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