Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21487
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dc.contributor.authorPrasad, K R K-
dc.contributor.authorJoshi, N N-
dc.date.accessioned2013-10-04T10:21:12Z-
dc.date.available2013-10-04T10:21:12Z-
dc.date.issued2003-01-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21487-
dc.description150-153en_US
dc.description.abstractVarious 1,3-oxazolidines have been prepared from norephedrine and aldehydes/ketones and the corresponding zinc amides prepared in situ have been utilized as catalysts for the enantioslective addition of diethylzinc to aryl aldehydes. Good enantioselectivities (73-85%) and consistent product configuration are realized in all the cases examined. A mechanism has been proposed that can account for the stereochemical outcome.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.42B(01) [January 2003]en_US
dc.titleChiral 1,3-oxazolidines as the ligands for the enantioselective addition of diethylzinc to aryl aldehydesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.42B(01) [January 2003]

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