Group 9 metal complex-catalyzed hydrogen transfer reactions and their application to organic synthesis

被引:7
|
作者
Fujita, Ken-ichi [1 ,2 ]
机构
[1] Kyoto Univ, Grad Sch Global Environm Studies, Sakyo Ku, Kyoto 6068501, Japan
[2] Kyoto Univ, Grad Sch Human & Environm Studies, Sakyo Ku, Kyoto 6068501, Japan
关键词
iridium catalyst; rhodium catalyst; Cp*ligand; oxidation; reduction; hydrogen transfer; alcohol; amine;
D O I
10.5059/yukigoseikyokaishi.66.322
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Development of methodology directed toward environmentally benign molecular transformations is one of the most important subjects in modern synthetic organic chemistry. As a promising method for environmentally benign transformation of organic molecules, we have focused on the transition metal catalyzed "Hydrogen Transfer Reactions". Here, we report our recent studies on hydrogen transfer reactions catalyzed by group 9 metal complexes bearing Cp* (eta(5)-pentamethylcyclopentadienyl) ligand and their application to organic synthesis, which include (1) Cp*Ir complex-catalyzed oxidation of alcohols, (2) Cp*Ir complex-catalyzed transfer hydrogenation of nitrogen heteroaromatics using 2-propanol as a hydrogen donor, (3) Cp*Ir complex-catalyzed carbon-nitrogen and carbon-carbon bond formation using alcohols as alkylating reagents, (4) Cp* Ir and Cp*Rh complex-catalyzed synthesis of nitrogen heterocycles by intra- and intermolecular carbon-nitrogen bond formation.
引用
收藏
页码:322 / 331
页数:10
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