| Literature DB >> 26622223 |
Gregory A Applegate1, David B Berkowitz1.
Abstract
Over the past two decades, the domains of both frontline synthetic organic chemistry and process chemistry and have seen an increase in crosstalk between asymmetric organic/organometallic approaches and enzymatic approaches to stereocontrolled synthesis. This review highlights the particularly auspicious role for dehydrogenase enzymes in this endeavor, with a focus on dynamic reductive kinetic resolutions (DYRKR) to "deracemize" building blocks, often setting two stereocenters in so doing. The scope and limitations of such dehydrogenase-mediated processes are overviewed, as are future possibilities for the evolution of enzymatic DYRKR.Entities:
Keywords: Asymmetric synthesis; biocatalysis; dehydrogenase enzymes; deracemization; dynamic kinetic resolution
Year: 2015 PMID: 26622223 PMCID: PMC4662550 DOI: 10.1002/adsc.201500316
Source DB: PubMed Journal: Adv Synth Catal ISSN: 1615-4150 Impact factor: 5.837