Literature DB >> 26622223

Exploiting Enzymatic Dynamic Reductive Kinetic Resolution (DYRKR) in Stereocontrolled Synthesis.

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


  54 in total

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7.  Asymmetric hydrogenation of α,α'-disubstituted cycloketones through dynamic kinetic resolution: an efficient construction of chiral diols with three contiguous stereocenters.

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Review 10.  Advances in the enzymatic reduction of ketones.

Authors:  Jeffrey C Moore; David J Pollard; Birgit Kosjek; Paul N Devine
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3.  Biocatalytic Parallel Interconnected Dynamic Asymmetric Disproportionation of α-Substituted Aldehydes: Atom-Efficient Access to Enantiopure (S)-Profens and Profenols.

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Journal:  Adv Synth Catal       Date:  2018-06-12       Impact factor: 5.837

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