Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21909
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dc.contributor.authorSharma, Utpal-
dc.contributor.authorBora, Utpal-
dc.contributor.authorChetia, Apurba-
dc.contributor.authorBoruah, Romesh C-
dc.contributor.authorSandhu, Jagir Singh-
dc.date.accessioned2013-10-11T10:42:39Z-
dc.date.available2013-10-11T10:42:39Z-
dc.date.issued2002-05-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21909-
dc.description1012-1014en_US
dc.description.abstractThe asymmetric 1,3-dipolar cycloaddition reaction of nitrile oxides 2a-b to olefins 1a-c has been acccomplished by employing pregnenol one as chiral auxiliary. The optically pure 3-aryl-5-isoxazoline esters 9 are obtained from the major diastereomer in good yield.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.41B(05) [May 2002]en_US
dc.titleRegio- and stereoselective synthesis of isoxazolines via cycloaddition reactions using pregnenolone as chiral auxiliaryen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.41B(05) [May 2002]

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