Biomimetic Ketone Reduction by Disulfide Radical Anion

The conversion of ribonucleosides to 2 '-deoxyribonucleosides is catalyzed by ribonucleoside reductase enzymes in nature. One of the key steps in this complex radical mechanism is the reduction of the 3 '-ketodeoxynucleotide by a pair of cysteine residues, providing the electrons via a disulfide radical anion (RSSR center dot-) in the active site of the enzyme. In the present study, the bioinspired conversion of ketones to corresponding alcohols was achieved by the intermediacy of disulfide radical anion of cysteine (CysSSCys)(center dot-) in water. High concentration of cysteine and pH 10.6 are necessary for high-yielding reactions. The photoinitiated radical chain reaction includes the one-electron reduction of carbonyl moiety by disulfide radical anion, protonation of the resulting ketyl radical anion by water, and H-atom abstraction from CysSH. The (CysSSCys)(center dot-) transient species generated by ionizing radiation in aqueous solutions allowed the measurement of kinetic data with ketones by pulse radiolysis. By measuring the rate of the decay of (CysSSCys)(center dot-) at lambda(max) = 420 nm at various concentrations of ketones, we found the rate constants of three cyclic ketones to be in the range of 10(4)-10(5) M(-1)s(-1) at similar to 22 degrees C.

Automated summary

The conversion of ribonucleosides to 2'-deoxyribonucleosides is catalyzed by ribonucleoside reductase enzymes. This study achieved the bioinspired conversion of ketones to alcohols through the intermediacy of disulfide radical anion of cysteine in water, with high concentrations of cysteine and pH 10.6 required for high-yielding reactions. The research also found that the rate constants of three cyclic ketones ranged from 10^4 to 10^5 M(-1)s(-1) at approximately 22 degrees C.