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dc.contributor.authorVijay Nair, G-
dc.contributor.authorAni Deepthi-
dc.contributor.authorManojkumar, P-
dc.contributor.authorBindu, S-
dc.contributor.authorSreekumar, V-
dc.contributor.authorBeneesh, P B-
dc.contributor.authorResmi Mohan-
dc.contributor.authorSuresh, E-
dc.date.accessioned2014-06-17T05:24:17Z-
dc.date.available2014-06-17T05:24:17Z-
dc.date.issued2006-
dc.identifier.citationJournal of Organic Chemistry 71(6):2313-2319;17 Mar 2006en_US
dc.identifier.issn0022-3263-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1532-
dc.description.abstractThe zwitterion formed by the reaction of dimethoxycarbene and DMAD adds efficiently to one of the carbonyl groups of 1,2-dicarbonyl compounds and anhydrides to generate dihydrofurans and spirodihydrofurans in good yields. In many cases, the carbene inserts into the C-C bond of the dione to yield masked vicinal tricarbonyl systems.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectMulticomponent reactionen_US
dc.subjectNucleophilic carbenesen_US
dc.subjectDimethyl butynedioateen_US
dc.subjectFacile synthesisen_US
dc.subjectElectrophilic styrenesen_US
dc.subjectVinyl isocyanatesen_US
dc.subject4+1 Cycloadditionen_US
dc.subjectDerivatives constructionen_US
dc.subjectBis(alkylthio)carbenesen_US
dc.titleReaction of dimethoxycarbene-DMAD zwitterion with 1,2-diones and anhydrides: A novel synthesis of highly substituted dihydrofurans and spirodihydrofuransen_US
dc.typeArticleen_US
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