Stereoselective bioreduction of 1-(5-phenylfuran-2-yl)-ethanones mediated by baker's yeast
Author:
Publisher
Informa UK Limited
Subject
Biochemistry,Catalysis,Biotechnology
Link
http://www.tandfonline.com/doi/pdf/10.3109/10242422.2011.638374
Reference24 articles.
1. Bencze LC, Paizs C, Toşa MI, Irimie FD. 2010. Substituent effects on the stereochemical outcome of the baker's yeast-mediated biotransformation of α-hydroxy- and α-acetoxymethyl-5-phenylfuran-2-yl-ethanones. Tetrahedron: Asymmetry; 21: 356–364.
2. Bencze LC, Paizs C, Toşa MI, Irimie FD. 2011. Sequential use of regio- and stereoselective lipases for the efficient kinetic resolution of racemic 1-(5-phenylfuran-2-yl)ethane-1,2-diols. Tetrahedron: Asymmetry; 22: 675–683.
3. Busto E, Gotor-Fernandez V, Gotor V. 2006. Biocatalytic preparation of optically active 4-(N,N-dimethylamino)pyridines for application in chemical asymmetric catalysis. Tetrahedron: Asymmetry; 17: 1007–1016.
4. Cui JN, Ema T, Sakai T, Utaka M. 1998. Control of enantioselectivity in the baker's yeast asymmetric reduction of γ-chloro β-diketones to γ-chloro (S)-β-hydroxy ketones. Tetrahedron: Asymmetry; 9: 2681–2692.
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