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Chapter 2 Chemical methods for the investigation of stereochemical problems in biology
Chapter 3 Stereochemistry of dehydrogenases
Chapter 4 Stereochemistry of pyridoxal phosphatecatalyzed reactions
Chapter 5 Stereochemistry of enzymatic substitution at phosphorus
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absolute configuration absorption acetate achiral aconitase active amino acid bathorhodopsin binding Biochem Biochemistry Biol Biophys bleaching Brändén carbon catalyzed CH3 CH3 Chem chemical chiral center chiral methyl chromophore citrate coenzyme cofactor complex compounds conformation COOH COOH decarboxylation determined deuterium diastereoisomeric diastereoisomers diastereomers diastereotopic dioldehydratase double bond enantiomeric enantiomers enzymatic enzyme hydrogen hydrogen atoms interactions intermediate inversion of configuration involved isocitrate isomerization isomers isotope kcal/mol kinase kinetic labelled liver alcohol dehydrogenase mechanism methyl group methylene molecular molecule mutase NADH NADPH nucleotides opsin optical phosphate phosphorothioate phosphorus phosphorylation position pro-R pro-S prochiral protein proton protonated Schiff base pyruvate racemic reaction resonance Raman retention retinal rhodopsin ring rotation samples Schiff base shown Si face specific spectra stereochemical stereochemical course stereochemistry stereoisomers stereospecific steric course structure studies substitution substrate subunit symmetry synthesis tion transaminase transfer tritium visual pigment analogs