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Stereoselective reduction of 2-substituted cyclohexanones by .I.Saccharomyces cerevisiae./I..

  1. 1.
    SYSNO ASEP0194770
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JOstatní články
    TitleStereoselective reduction of 2-substituted cyclohexanones by .I.Saccharomyces cerevisiae./I..
    Author(s) Zarevúcka, Marie (UOCHB-X) RID
    Reitmayerová, Pavla (UOCHB-X)
    Wimmer, Zdeněk (UOCHB-X)
    Šaman, David (UOCHB-X) RID, ORCID
    Source TitleBiotechnology Letters. - : Springer - ISSN 0141-5492
    Roč. 25, - (2003), s. 987-992
    Number of pages6 s.
    Languageeng - English
    CountryGB - United Kingdom
    Keywordsbioreactor ; enantiomer ; enzymic reduction
    Subject RIVCC - Organic Chemistry
    R&D ProjectsIBS4055104 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    CEZAV0Z4055905 - UOCHB-X
    AnnotationA comparative study of two modifications of enzymic reduction of ethyl .I.N./I.-{2-{4-[(2-oxo-cyclohexyl)methyl]phenoxy}ethyl} carbamate (1), an insect juvenile hormone bioanalog, was performed using .I.Saccharomyces cerevisiae./I. in two bioreactors of different size, 250-ml shake-flask and 1-l fermenter.
    WorkplaceInstitute of Organic Chemistry and Biochemistry
    Contactasep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Jana Procházková, Tel.: 220 183 418
    Year of Publishing2004

Number of the records: 1  

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