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dc.contributor.authorBanerji, Avijit-
dc.contributor.authorHaldar (nee Datta), Sunanda-
dc.contributor.authorBanerji, Julie-
dc.date.accessioned2013-03-24T13:02:32Z-
dc.date.available2013-03-24T13:02:32Z-
dc.date.issued1999-06-
dc.identifier.urihttp://hdl.handle.net/123456789/16458-
dc.description641-647en_US
dc.description.abstractCycloaddition reactions of 1-phenyl-3-oxidopyridinium betaine with a number of 1,2-disubstituted olefins bearing electron-withdrawing groups have been investigated. The regio-and stereochemical preferences of the cycloaddition processes have been studied. A Michael addition product derived from a cycloadduct isalso obtained in addition to the cyeloadducts.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(06) [June 1999]en_US
dc.title1,3-Dipolar cycloadditions : Part IV1,2 - Cycloaddition of 1-phenyl-3-oxidopyridinium betaines to electron-deficient alkenesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.38B(06) [June 1999]

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