Number of the records: 1  

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

  1. 1.
    0194770 - UOCHB-X 20030075 RIV GB eng J - Journal Article
    Zarevúcka, Marie - Reitmayerová, Pavla - Wimmer, Zdeněk - Šaman, David
    Stereoselective reduction of 2-substituted cyclohexanones by .I.Saccharomyces cerevisiae./I.
    Biotechnology Letters. Roč. 25, - (2003), s. 987-992. ISSN 0141-5492. E-ISSN 1573-6776
    R&D Projects: GA AV ČR IBS4055104
    Institutional research plan: CEZ:AV0Z4055905
    Keywords : bioreactor * enantiomer * enzymic reduction
    Subject RIV: CC - Organic Chemistry
    Impact factor: 0.778, year: 2003

    A 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.
    Permanent Link: http://hdl.handle.net/11104/0090441
     

Number of the records: 1  

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