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dc.contributor.authorVijay Nair, G-
dc.contributor.authorDhanya, R-
dc.contributor.authorVidya, N-
dc.contributor.authorDevipriya, S-
dc.date.accessioned2017-02-02T10:59:04Z-
dc.date.available2017-02-02T10:59:04Z-
dc.date.issued2006-
dc.identifier.citationSynthesis - Stuttgart, (1):107-110en_US
dc.identifier.urihttp://hdl.handle.net/123456789/2645-
dc.description.abstractLewis acid promoted addition of allylsilane to o-qui­nonediimines afforded tetrahydroquinoxaline derivatives or allyl­ated amides, depending on the nature of the substituent on the imine nitrogen.en_US
dc.language.isoenen_US
dc.publisherThiemeen_US
dc.subjecto-quinonediimidesen_US
dc.subjectallyltriisopropylsilaneen_US
dc.subjectLewis acidsen_US
dc.subjecttetrahydroquinoxalinesen_US
dc.subjectallylated amidesen_US
dc.titleLewis Acid Catalyzed Addition of Allylsilane to o-Quinonediimides: Formal Diels-Alder Reaction Versus Allylationen_US
dc.typeArticleen_US
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