Molecules | |
Experimental and Theoretical Perspectives of the Noyori-Ikariya Asymmetric Transfer Hydrogenation of Imines | |
Jan Pecháček1  Beáta Vilhanová1  Ondřej Matuška1  Jiří Václavík1  Petr Šot1  Petr Kačer1  Marek Kuzma2  | |
[1] Department of Organic Technology, Institute of Chemical Technology, Technická 5,CZ-166 28 Prague, Czech Republic;Laboratory of Molecular Structure Characterization, Institute of Microbiology, v.v.i.,Academy of Sciences of the Czech Republic, Vídeňská 1083, CZ-142 20 Prague, Czech Republic; | |
关键词: ruthenium; asymmetric hydrogenation; imine; ligand; sulfonyl; arene; DFT; | |
DOI : 10.3390/molecules19066987 | |
来源: DOAJ |
【 摘 要 】
The asymmetric transfer hydrogenation (ATH) of imines catalyzed by the Noyori-Ikariya [RuCl(η6-arene)(N-arylsulfonyl-DPEN)] (DPEN = 1,2-diphenylethylene-1,2-diamine) half-sandwich complexes is a research topic that is still being intensively developed. This article focuses on selected aspects of this catalytic system. First, a great deal of attention is devoted to the N-arylsulfonyl moiety of the catalysts in termsof its interaction with protonated imines (substrates) and amines (components of thehydrogen-donor mixture). The second part is oriented toward the role of the η6-coordinated arene. The final part concerns the imine substrate structural modifications and their importance in connection with ATH. Throughout the text, the summary of known findings is complemented with newly-presented ones, which have been approached both experimentally and computationally.
【 授权许可】
Unknown