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Lewis Acid Catalyzed Addition of Allylsilane to o-Quinonediimides: Formal Diels-Alder Reaction Versus Allylation

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dc.contributor.author Vijay Nair, G
dc.contributor.author Dhanya, R
dc.contributor.author Vidya, N
dc.contributor.author Devipriya, S
dc.date.accessioned 2017-02-02T10:59:04Z
dc.date.available 2017-02-02T10:59:04Z
dc.date.issued 2006
dc.identifier.citation Synthesis - Stuttgart, (1):107-110 en_US
dc.identifier.uri http://hdl.handle.net/123456789/2645
dc.description.abstract Lewis 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.iso en en_US
dc.publisher Thieme en_US
dc.subject o-quinonediimides en_US
dc.subject allyltriisopropylsilane en_US
dc.subject Lewis acids en_US
dc.subject tetrahydroquinoxalines en_US
dc.subject allylated amides en_US
dc.title Lewis Acid Catalyzed Addition of Allylsilane to o-Quinonediimides: Formal Diels-Alder Reaction Versus Allylation en_US
dc.type Article en_US


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