Electrochemically Promoted Asymmetric Transfer Hydrogenation of 2,2,2-Trifluoroacetophenone.

The study reported an electrochemically promoted asymmetric hydrogen transfer reaction of 2,2,2-trifluoroacetophenone with a chiral Ru complex. (R)-α-(Trifluoromethyl) benzyl alcohol with a 96% yield and 94% ee could be obtained with only a 0.5 F mol-1 charge amount at room temperature and normal pressure.

One-Pot Synthesis of d-Phenylalanine-Functionalized Multiwalled Carbon Nanotubes: A Metal-Free Chiral Material for the Asymmetric Electroreduction of Aromatic Ketones.

A simple protocol to synthesize d-phenylalanine (d-PHE)-functionalized multiwalled carbon nanotubes (MWCNTs) via the one-pot method was established by grafting d-PHE onto MWCNTs to obtain d-PHE-MWCNTs under mild reaction conditions. The resulting d-PHE-MWCNTs were characterized in detail via spectroscopy and surface analysis. The electroreduction of 2,2,2-trifluoroacetophenone at the d-PHE-MWCNTs cathode afforded ( S)-α-(trifluoromethyl) benzyl alcohol whose yield was 65% and the enantiomeric excess was 40%. No extra catalysts were required in this electrochemical reaction solution compared with other reactions requiring homogeneous catalysis. The metal-free chiral material also showed acceptable asymmetric electroreduction performance, considerable stability, and favorable reusability.

Entrapment of a chiral cobalt complex within silver: a novel heterogeneous catalyst for asymmetric carboxylation of benzyl bromides with CO2.

A novel way to accommodate heterogeneous catalysis, CO2 fixation and asymmetric synthesis on one catalyst is reported. The [Co]@Ag composite was prepared for the first time and used for asymmetric carboxylation of benzyl bromides with CO2. All the procedures were performed under mild conditions. Moreover, the [Co]@Ag composite has terrific stability and reusability.