Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/22462
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dc.contributor.authorChary, K Purushothama-
dc.contributor.authorThomas, R Mathew-
dc.contributor.authorIyengar, D S-
dc.date.accessioned2013-10-22T11:52:16Z-
dc.date.available2013-10-22T11:52:16Z-
dc.date.issued2000-01-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/22462-
dc.description57-59en_US
dc.description.abstractEnantioselective reduction of prochiral ketones has been achieved by the combination of NaBH4/ZrCl4 and (S)(-)-α,α-diphenyl prolinol in moderate to high enantiomeric excess.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.39B(01) [January 2000]en_US
dc.titleChirally modified NaBH4/ZrCl4 promoted asymmetric reduction of prochiral ketones†en_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.39B(01) [January 2000]

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