Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/55448
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dc.contributor.authorChanysheva, Aliya R-
dc.contributor.authorZorin, Vladimir V-
dc.date.accessioned2020-10-09T05:19:50Z-
dc.date.available2020-10-09T05:19:50Z-
dc.date.issued2020-09-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/55448-
dc.description1381-1383en_US
dc.description.abstractSynthesis of enantiomerically pure (2S)-(+)-heptan-2-ol and (2S)-(+)-octan-2-ol by bioreduction of heptan-2-one and octan-2-one using Daucus carota cells has been studied. Optimization of bioreduction conditions has been carried out in the presence of various exogenous reducing agents (ethanol, isopropanol, glucose). Conditions allowing to obtain (2S)-(+)-heptan-2-ol with 91% yield and optical purity 98% ee and (2S)-(+)-octan-2-ol in 95% yield and > 99% ee have been found.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.59B(09) [September 2020]en_US
dc.subjectDaucus carotaen_US
dc.subjectBioreductionen_US
dc.subjectExogenous reducing agentsen_US
dc.subject(2S)-(+)-heptan-2-olen_US
dc.subject(2S)-(+)-octan-2-olen_US
dc.titleEnantioselective bioreduction of heptan-2-one and octan-2-one catalyzed by Daucus carota cellsen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.59B(09) [September 2020]

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