Number of the records: 1
Stereoselective reduction of 2-substituted cyclohexanones by .I.Saccharomyces cerevisiae./I..
- 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