Publication | Closed Access
Two Steps in One Pot: Enzyme Cascade for the Synthesis of Nor(pseudo)ephedrine from Inexpensive Starting Materials
186
Citations
22
References
2013
Year
Bioorganic ChemistryEngineeringOrganic ChemistryEnzymatic ModificationMedicinal ChemistryBiosynthesisEnzyme CascadeStereoselective SynthesisOnline DeliveryBiochemistryTechnical Support IssuesCatalysisSynthesis MethodPharmacologyNatural Product SynthesisEnantioselective SynthesisBiomolecular EngineeringCellular EnzymologyNatural SciencesEnzyme CatalysisEnzyme Cascade ConsistingSynthetic Chemistry
Two steps in one pot: An enzyme cascade consisting of a lyase and an (R)- or (S)-selective ω-transaminase (TA) provides (1R,2R)-norpseudoephedrine and (1R,2S)-norephedrine in only two steps. The intermediate is not isolated in this one-pot reaction and the products are obtained in high enantio- and diastereomeric purity. Moreover, the by-product from the second reaction can be recycled to serve as the substrate for the first reaction. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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