A convenient enantioselective synthesis of trans-2-aryloxycyclohexan-1-ols using pig liver acetone powder (PLAP) as biocatalyst

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Krishna, Peddinti Rama
dc.contributor.author Bharathi, Tirumala K.
dc.date.accessioned 2022-03-27T09:04:32Z
dc.date.available 2022-03-27T09:04:32Z
dc.date.issued 1995-01-01
dc.description.abstract Pig liver acetone powder (PLAP) has been used as a biocatalyst for enantioselective hydrolysis of racemic trans-1-acetoxy-2-aryloxycyclohexannes to produce the resulting (R,R)-2-aryloxycyclohexan-1-ols upto > 99% enantiomeric purities. (R,R)-Selectivity in this hydrolysis of racemic trans-2-aryloxycyclohexyl acetates was explained on the basis of Jones' three dimensional active site-model. © 1995.
dc.identifier.citation Tetrahedron: Asymmetry. v.6(2)
dc.identifier.issn 09574166
dc.identifier.uri 10.1016/0957-4166(95)00029-O
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/095741669500029O
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12373
dc.title A convenient enantioselective synthesis of trans-2-aryloxycyclohexan-1-ols using pig liver acetone powder (PLAP) as biocatalyst
dc.type Journal. Article
dspace.entity.type
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