Enantioselective reduction of substituted acetophenones by Aspergillus niger

Kurbanoğlu, Namudar İzzet; Kılıç, Harun

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dc.contributor.authors	Kurbanoglu, EB; Zilbeyaz, K; Kurbanoglu, NI; Kilic, H;
dc.date.accessioned	2020-02-27T08:30:10Z
dc.date.available	2020-02-27T08:30:10Z
dc.date.issued	2007
dc.identifier.citation	Kurbanoglu, EB; Zilbeyaz, K; Kurbanoglu, NI; Kilic, H; (2007). Enantioselective reduction of substituted acetophenones by Aspergillus niger. TETRAHEDRON-ASYMMETRY, 18, 1162-1159
dc.identifier.issn	0957-4166
dc.identifier.uri	https://doi.org/10.1016/j.tetasy.2007.05.017
dc.identifier.uri	https://hdl.handle.net/20.500.12619/66194
dc.description.abstract	Fourteen strains of Aspergillus niger were isolated from soil samples. These isolates were evaluated for tile reduction of acetophenone to 1-phenylethanol. Among the tested isolates, whole cells of the A. niger EBK-9 isolate were found to be an effective biocatalyst for the enantioselective reduction of acetophenone. Under optimized conditions substituted acetophenones were converted to the corresponding optically active alcohol in up to 99% ee. (C) 2007 Elsevier Ltd. All rights reserved.
dc.language	English
dc.publisher	PERGAMON-ELSEVIER SCIENCE LTD
dc.subject	Chemistry
dc.title	Enantioselective reduction of substituted acetophenones by Aspergillus niger
dc.type	Article
dc.identifier.volume	18
dc.identifier.startpage	1159
dc.identifier.endpage	1162
dc.contributor.department	Sakarya Üniversitesi/Eğitim Fakültesi/Matematik Ve Fen Bilimleri Eğitimi Bölümü
dc.contributor.saüauthor	Kurbanoğlu, Namudar İzzet
dc.contributor.saüauthor	Kılıç, Harun
dc.relation.journal	TETRAHEDRON-ASYMMETRY
dc.identifier.wos	WOS:000248103800002
dc.identifier.doi	10.1016/j.tetasy.2007.05.017
dc.contributor.author	Kurbanoğlu, Namudar İzzet
dc.contributor.author	Kılıç, Harun