Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/6863
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dc.contributor.authorSharma, Raman K-
dc.contributor.authorAggarwal, Neha-
dc.contributor.authorArya, Anu-
dc.contributor.authorOlsen, Carl E-
dc.contributor.authorParmar, Virinder S-
dc.contributor.authorPrasad, Ashok K-
dc.date.accessioned2009-12-11T05:57:25Z-
dc.date.available2009-12-11T05:57:25Z-
dc.date.issued2009-12-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/6863-
dc.description1727-1731en_US
dc.description.abstractEfficient regio- and stereoselective deacylation of acyloxy function involving C-5′ hydroxyl group of -anomer over the other similar C-5′ acyl group of -anomer and acyl groups involving secondary hydroxyls in anomeric mixture of peracylates of D-ribose has been achieved during deacylation reaction mediated by Lipozyme® TL IM (Thermomyces lanuginosus lipase immobilized on silica). This enzymatic methodology has been efficiently used for the separation of anomeric mixtures of peracylated ,-D-ribofuranosides.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJC-B Vol.48B(12) December 2009]en_US
dc.subjectAnomeric mixtureen_US
dc.subjectLipozyme® TL IMen_US
dc.subjectperacylated ,-D-ribofuranosidesen_US
dc.subjectregio- and stereo- ­selective deacylationen_US
dc.titleLipase-catalyzed regio- and stereoselective deacylation: Separation of anomers of peracylated , -D-ribofuranosidesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.48B(12) December 2009]

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