Publication | Closed Access
Expanding the reaction space of aldolases using hydroxypyruvate as a nucleophilic substrate
33
Citations
45
References
2016
Year
Bioorganic ChemistryAldo-keto ReductaseMolecular BiologyChemical BiologyRedox BiologyBiosynthesisBioenergeticsStructure-function Enzyme KineticsReaction SpaceNucleophilic SubstrateAldehyde DehydrogenaseBiochemistryBiocatalysisBiomolecular EngineeringNatural SciencesEnzyme CatalysisMetabolismMedicineCarbonyl Metabolism
Hydroxypyruvate was shown to be a nucleophile for class II pyruvate aldolases isolated from biodiversity, allowing unprecedented stereoselective cross-aldol reactions.
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