Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/9105
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dc.contributor.authorPardasani, R T-
dc.contributor.authorPardasani, P-
dc.contributor.authorGupta, B-
dc.contributor.authorLondhe, A V-
dc.contributor.authorKohli, S-
dc.date.accessioned2010-05-31T09:47:39Z-
dc.date.available2010-05-31T09:47:39Z-
dc.date.issued2005-06-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/9105-
dc.description1252-1256en_US
dc.description.abstractThe Knovenaegel type condensation of benzo[b]thiophene-2,3-dione (thioisatin), indol-2,3-dione and acenaphthylene-1,2-dione with imidazolidine, oxazolidine, pyrimidinetrione and thiazolidine derivatives has been described: The newly synthesized products have been characterized by spectral techniques (IR, 1H NMR, 13C NMR and mass). Correlation of experimental results and exclusive formation of anti-monocondensation products has been ascertained on the basis of semiempirical calculations.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 Den_US
dc.sourceIJC-B Vol.44B(06) [June 2005]en_US
dc.titleSynthesis and semiempirical calculations of isatylidine, thioisatylidine and acenaphthylidine derivatives of imidazolidine, thiazolidine, oxazolidine and pyrimidinetrioneen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.44B(06) [June 2005]

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