Asymmetric transfer hydrogenation of γ-aryl α,γ-dioxo-butyric acid esters

The asymmetric transfer hydrogenation (ATH) of a series of γ-aryl-α,γ-dioxo-butyric acid esters has been accomplished smoothly. Six ferrocene-based chiral ligands have been prepared and applied in the reactions respectively. Simultaneously, enantiopure Ts-DPEN's utilization in the ATH also has...

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Veröffentlicht in:RSC advances 2016-01, Vol.6 (39), p.33126-33131
Hauptverfasser: Mo, Yuan-Zhao, Nie, Hui-Fang, Lei, Yang, Zhang, Dong-Xu, Li, Xiao-Ye, Zhang, Sheng-Yong, Wang, Qiao-Feng
Format: Artikel
Sprache:eng
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Zusammenfassung:The asymmetric transfer hydrogenation (ATH) of a series of γ-aryl-α,γ-dioxo-butyric acid esters has been accomplished smoothly. Six ferrocene-based chiral ligands have been prepared and applied in the reactions respectively. Simultaneously, enantiopure Ts-DPEN's utilization in the ATH also has been investigated and the products were obtained in 30-85% chemical yields with 37-95.5% ee. Six ferrocene-based chiral ligands were prepared and applied in ATH reaction of multiple-carbonyl compounds as RuCl( p -cymene)[Ts-DPEN] did.
ISSN:2046-2069
2046-2069
DOI:10.1039/c6ra02500e