Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/30538
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dc.contributor.authorPadmavathi, V-
dc.contributor.authorSudheer, K-
dc.contributor.authorMuralikrishna, A-
dc.contributor.authorPadmaja, A-
dc.date.accessioned2015-02-12T09:14:00Z-
dc.date.available2015-02-12T09:14:00Z-
dc.date.issued2015-02-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/30538-
dc.description283-289en_US
dc.description.abstractThe gem cyano ester functionality in double Michael adduct, 4-carboethoxy-2-carbomethoxy-4-cyano-3,5-diaryltetra-hydro[2H]thiopyran-1,1-dioxide 1 has been exploited to develop three different types of spiro heterocycles viz., spiro pyrimidine, pyrazole and isoxazole derivatives in the presence of appropriate nucleophiles.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.54B(02) [February 2015]en_US
dc.subjectSpiro-pyrimidinesen_US
dc.subjectSpiro-pyrazolesen_US
dc.subjectSpiro-isoxazolesen_US
dc.subjectCyclocondensationen_US
dc.subjectPiperidineen_US
dc.titleDouble Michael adducts: Source for spiro heterocyclesen_US
dc.typeArticleen_US
Appears in Collections: IJC-B Vol.54B(02) [February 2015]

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