Literature DB >> 12943849

Controlling chirality.

Nicholas J Turner1.   

Abstract

New strategies are continually being developed for using enzymes to efficiently catalyse the enantioselective synthesis of chiral non-racemic compounds. Alternatives to asymmetric synthesis or kinetic resolution include dynamic kinetic resolution, deracemisation and enantioconvergent transformations. Moreover, a much greater understanding is being developed of the parameters that can affect the stereochemical outcome of the reaction (e.g. solvent, substrate design, immobilization and directed evolution).

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Year:  2003        PMID: 12943849     DOI: 10.1016/s0958-1669(03)00093-4

Source DB:  PubMed          Journal:  Curr Opin Biotechnol        ISSN: 0958-1669            Impact factor:   9.740


  3 in total

1.  Highly L and D enantioselective variants of horseradish peroxidase discovered by an ultrahigh-throughput selection method.

Authors:  Eugene Antipov; Art E Cho; K Dane Wittrup; Alexander M Klibanov
Journal:  Proc Natl Acad Sci U S A       Date:  2008-11-12       Impact factor: 11.205

2.  How a single-point mutation in horseradish peroxidase markedly enhances enantioselectivity.

Authors:  Eugene Antipov; Art E Cho; Alexander M Klibanov
Journal:  J Am Chem Soc       Date:  2009-08-12       Impact factor: 15.419

3.  Substrate control in stereoselective lanthionine biosynthesis.

Authors:  Weixin Tang; Gonzalo Jiménez-Osés; K N Houk; Wilfred A van der Donk
Journal:  Nat Chem       Date:  2014-11-24       Impact factor: 24.427

  3 in total

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