Asymmetric synthesis of diverse glycolic acid scaffolds via dynamic kinetic resolution of α-keto esters

Journal of the American Chemical Society

Volumn 134, Issue 49, 2012, Pages 20197-20206

  Steward, Kimberly M ^a   Corbett, Michael T ^a   Goodman, C Guy ^a   Johnson, Jeffrey S ^a  

^a University of North Carolina at Chapel Hill   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ASYMMETRIC SYNTHESIS; ASYMMETRIC TRANSFER HYDROGENATION; CARBOXYLIC ACID DERIVATIVES; DYNAMIC KINETIC RESOLUTION; ENANTIOCONTROL; GLYCOLIC ACIDS; HIGH AFFINITY; KETO ESTER; STEREOSELECTIVE CONSTRUCTION;

CARBOXYLIC ACIDS; ESTERS; RUTHENIUM COMPOUNDS; SCAFFOLDS;

ESTERIFICATION;

ALPHA KETO ESTER; CARBOXYLIC ACID DERIVATIVE; ESTER DERIVATIVE; GLYCOLIC ACID; META TERPHENYLSULFONAMIDE; MOLECULAR SCAFFOLD; SULFONAMIDE; UNCLASSIFIED DRUG;

ARTICLE; ASYMMETRIC SYNTHESIS; BINDING AFFINITY; CHEMICAL REACTION KINETICS; CONTROLLED STUDY; DIASTEREOISOMER; DYNAMIC KINETIC RESOLUTION; ENANTIOMER; ENANTIOSELECTIVITY; HYDROGENATION; HYDROXYLATION; REDUCTION; STEREOCHEMISTRY; SUBSTITUTION REACTION;

ESTERS; GLYCOLATES; HYDROGENATION; KETONES; KINETICS; MOLECULAR CONFORMATION; STEREOISOMERISM; THERMODYNAMICS;

EID: 84870955294     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja3102709     Document Type: Article

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