1373610-41-3Relevant academic research and scientific papers
Dynamic kinetic resolution of α-keto esters via asymmetric transfer hydrogenation
Steward, Kimberly M.,Gentry, Emily C.,Johnson, Jeffrey S.
supporting information; experimental part, p. 7329 - 7332 (2012/06/16)
The dynamic kinetic resolution of β-aryl α-keto esters has been accomplished using a newly designed (arene)RuCl(monosulfonamide) transfer hydrogenation catalyst. This dynamic process generates three contiguous stereocenters with remarkable diastereoselect
Asymmetric synthesis of diverse glycolic acid scaffolds via dynamic kinetic resolution of α-keto esters
Steward, Kimberly M.,Corbett, Michael T.,Goodman, C. Guy,Johnson, Jeffrey S.
supporting information, p. 20197 - 20206 (2013/02/23)
The dynamic kinetic resolution of α-keto esters via asymmetric transfer hydrogenation has been developed as a technique for the highly stereoselective construction of structurally diverse β-substituted-α- hydroxy carboxylic acid derivatives. Through the development of a privileged m-terphenylsulfonamide for (arene)RuCl(monosulfonamide) complexes with a high affinity for selective α-keto ester reduction, excellent levels of chemo-, diastereo-, and enantiocontrol can be realized in the reduction of β-aryl- and β-chloro-α-keto esters.
