Applications of liver acetone powders in enantioselective synthesis

dc.contributor.author Basavaiah, Deevi
dc.date.accessioned 2022-03-27T09:03:01Z
dc.date.available 2022-03-27T09:03:01Z
dc.date.issued 2001-12-01
dc.description.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.
dc.identifier.citation Arkivoc. v.2001(8)
dc.identifier.issn 14246376
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12331
dc.title Applications of liver acetone powders in enantioselective synthesis
dc.type Journal. Article
dspace.entity.type
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