Basavaiah, Deevi (2001) Applications of liver acetone powders in enantioselective synthesis Arkivoc . pp. 70-82. ISSN 1424-6376
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Abstract
Applications of liver acetone powders (crude enzymes) as possible substitutes for purified enzyme preparations, hydrolases, in enantioselective organic transformations have been systematically investigated. (1R, 2R)-2-(4-Alkylphenoxy)cyclohexan-1-ols, (1R, 2R)- & (1S, 2S)- 2-nitroxycyclohexan-1-ols, (1R, 2S)-2-arylcyclohexan-1-ols, (3R, 4R)-6-methyl-3-phenylhept-1- en-4-ol, and (R)-1-(naphth-1-yl)ethanol have been synthesized in enantiomerically pure form via the enantioselective hydrolysis of the corresponding racemic acetates mediated by liver acetone powders.
Item Type: | Article |
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Source: | Copyright of this article belongs to Arkat USA Inc. |
Keywords: | Liver Acetone Powders; Enantioselective Synthesis; Enzymes |
ID Code: | 3902 |
Deposited On: | 18 Oct 2010 10:23 |
Last Modified: | 16 May 2016 14:36 |
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