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dc.contributor.authorSyam, Sujata-
dc.contributor.authorRane, Monica D-
dc.contributor.authorBhat, Sujata V-
dc.date.accessioned2008-08-28T11:29:50Z-
dc.date.available2008-08-28T11:29:50Z-
dc.date.issued2008-08-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/1923-
dc.description1308-1310en_US
dc.description.abstractSynthesis of optically pure 2,6-dimethyl-5-hepten-1-ol (melonol) has been attempted using lipases. Among three different lipases tested, pig pancreatic lipase (PPL) is found to be suitable for transesterification of (±)-melonol to afford (R)-(+)-melonol with an enantiomeric excess of 94%.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJCB Vol.47B(8) [August 2008]en_US
dc.subjectAsymmetric synthesisen_US
dc.subjectMelonolen_US
dc.subjectLipasesen_US
dc.subjectTransesterificationen_US
dc.subjectHydrolysisen_US
dc.titleLipase catalyzed asymmetric synthesis of (R)-melonolen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.47B(08) [August 2008]

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