Efficient reductive desymmetrization of bulky 1,3-cyclodiketones enabled by structure-guided directed evolution of a carbonyl reductase-Reference-Cited by-同舟云学术

Efficient reductive desymmetrization of bulky 1,3-cyclodiketones enabled by structure-guided directed evolution of a carbonyl reductase

Published:2019-10 Issue:10 Volume:2 Page:931-941
ISSN:2520-1158
Container-title:Nature Catalysis
language:en
Short-container-title:Nat Catal

Author:

Chen Xi^ORCID,Zhang Hongliu,Maria-Solano Miguel A.,Liu Weidong^ORCID,Li Juan,Feng Jinhui,Liu Xiangtao,Osuna Sílvia,Guo Rey-Ting^ORCID,Wu Qiaqing^ORCID,Zhu Dunming^ORCID,Ma Yanhe

Publisher

Springer Science and Business Media LLC

Subject

Process Chemistry and Technology,Biochemistry,Bioengineering,Catalysis

Link

http://www.nature.com/articles/s41929-019-0347-y.pdf

Reference67 articles.

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3. Paul, C. E., Lavandera, I., Gotor-Fernández, V., Kroutil, W. & Gotor, V. Escherichia coli/ADH-A: an all-inclusive catalyst for the selective biooxidation and deracemisation of secondary alcohols. ChemCatChem 5, 3875–3881 (2013).

4. Díaz-Rodríguez, A., Iglesias-Fernández, J., Rovira, C. & Gotor-Fernández, V. Enantioselective preparation of δ-valerolactones with horse liver alcohol dehydrogenase. ChemCatChem 6, 977–980 (2014).

5. Skoupi, M., Vaxelaire, C., Strohmann, C., Christmann, M. & Niemeyer, C. M. Enantiogroup-differentiating biocatalytic reductions of prochiral Cs-symmetrical dicarbonyl compounds to meso Compounds. Chem. Eur. J. 21, 8701–8705 (2015).

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