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dc.contributor.authorKumar, R Nandha-
dc.contributor.authorSuresh, T-
dc.contributor.authorDhanabal, T-
dc.contributor.authorMohan, P S-
dc.date.accessioned2008-04-01T11:38:06Z-
dc.date.available2008-04-01T11:38:06Z-
dc.date.issued2007-06-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/642-
dc.description995-1000en_US
dc.description.abstractThe Vilsmeier Haack reaction on 4-hydroxyquinaldines lead to potential intermediate 4-chloro-3-formyl-2-(2-hydroxy-ethene-1-yl) quinolines. The intermediate is further utilized to prepare quino[3,2-e][1,3]diazocines on treatment with thiourea. The structures of the new compounds are determined by the analytical and spectroscopic data.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJCB Vol.46B(6) [June 2007]en_US
dc.subjectVilsmeier Haack reactionen_US
dc.subject4-Hydroxyquinaldinesen_US
dc.subjectDiazocinesen_US
dc.titleA novel approach to 12-chloro-3-thio-4H-quino [3,2-e][1,3]diazocines via Vilsmeier Haack reactionen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.46B(06) [June 2007]

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