Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16308
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dc.contributor.authorSingal, Kewal Krishan-
dc.contributor.authorSingh, Baldev-
dc.date.accessioned2013-03-09T10:47:05Z-
dc.date.available2013-03-09T10:47:05Z-
dc.date.issued1999-03-
dc.identifier.urihttp://hdl.handle.net/123456789/16308-
dc.description292-296en_US
dc.description.abstract1,3-Dipolar cycloaddition of substituted open-chain conjugated azomethine N-oxides 1 with substituted N-arylmaleimides 2 leads  to the synthesis of new stereoisomeric 2,5-diaryl-3-(o-nitro)-styryl-4H-2,3,3a,5,6,6a-hexahydropyrrolo [3,4-d] isoxazole-4,6-dione derivatives 3 in excellent yield. These stereoisomers have been characterized as cis-3A and trans-3B on the basis of their spectral measurements and are obtained in the ratio of almost 1:2 respectively in all the reaction, which is the reverse of the stereoisomers obtained through the 'Huisgen reaction’ of C,N-diaryl nitrones with N-aryl maleimides as reported earlier from these laboratories.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.38B(03) [March 1999]en_US
dc.title1,3-Dipolar cycloaddition reactions of substituted open-chain conjugated azomethine N-oxides with substituted N-arylmaleimides leading to the synthesis of new stereoisomeric 2,5 -diaryl-3- (o-nitro)-styryl -4H-2,3,3a,5,6,6a- hexahydropyrrolo [3,4-d] isoxazole-4, 6-dione derivativesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.38B(03) [March 1999]

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