Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/9125
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dc.contributor.authorKaur, Jaspreet-
dc.contributor.authorSingh, Baldev-
dc.contributor.authorSingal, Kewal Krishan-
dc.date.accessioned2010-05-31T09:58:45Z-
dc.date.available2010-05-31T09:58:45Z-
dc.date.issued2005-07-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/9125-
dc.description1476-1480en_US
dc.description.abstract1,3-Dipolar cycloaddition reaction of variously substituted aldonitrones with N-benzyl maleimide leads to the synthesis of substituted 2, 3-diaryl-5-benzyl-2H-3, 3a, 4, 5, 6, 6a-hexahydropyrrolo[3, 4-d] isoxazole-4, 6-diones in good yield. Structures and stereochemistry of the products have been determined by detailed spectral studies.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 Den_US
dc.sourceIJC-B Vol.44B(07) [July 2005]en_US
dc.subjectHuisgen reactionen_US
dc.subjectaldonitronesen_US
dc.subjectN-benzyl maleimideen_US
dc.subjectisoxazole dionesen_US
dc.subjectstereochemistryen_US
dc.title‘Huisgen reaction’ of aldonitrones with N-benzyl maleimide leading to synthesis of 2, 3-diaryl-5-benzyl-2H-3, 3a, 4, 5, 6, 6a-hexahydropyrrolo[3, 4-d]isoxazole- 4, 6-dionesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.44B(07) [July 2005]

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