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Nuclease p1: a new biocatalyst for direct asymmetric aldol reaction under solvent-free conditions
78
Citations
34
References
2010
Year
EngineeringAldo-keto ReductaseMolecular BiologyOrganic ChemistryEnzymatic ModificationBiosynthesisBiochemical EngineeringNatural Product BiosynthesisSolvent-free ConditionsBiochemistryBiocatalysisCyclic KetonesNew BiocatalystCatalysisNatural Product SynthesisAsymmetric CatalysisUnnatural AbilityBiomolecular EngineeringNatural SciencesEnzyme CatalysisNuclease P1
The unnatural ability of nuclease p1 from Penicillium citrinum was first discovered to catalyze asymmetric aldol reactions between aromatic aldehydes and cyclic ketones under solvent-free conditions. The excellent enantioselectivities of up to 99% ee and high diastereoselectivities of up to >99 : 1 (anti/syn) were achieved. This nuclease p1 catalyzed reaction provided a novel case for new activities of existing enzymes, which widens the applicability of this biocatalyst in organic synthesis.
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