Intramolecular 1,3-Dipolar Cycloaddition of Azomethine Ylides Leading to Pyrido[2,3-b]quinolines

By Toth Judit   Somfai Barbara   Blasko Gabor   Dancso Andras   Toke Laszlo   Nyerges Miklos  

Synthetic Communications, Vol. 39, Iss. 13, 2009-01 ,pp. : 2258-2270

Taylor & Francis Ltd

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Intramolecular 1,3-Dipolar Cycloaddition of Geminal Difluoro Azomethine Ylides at Multiple Carbon-Carbon Bonds

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Russian Journal of Organic Chemistry, Vol. 41, Iss. 3, 2005-03 ,pp. : 361-369

MAIK Nauka/Interperiodica

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1,3-dipolar cycloaddition of fluorinated azomethine ylides at the C=N bond

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Russian Journal of Organic Chemistry, Vol. 40, Iss. 10, 2004-10 ,pp. : 1493-1499

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New Tandem Reactions of Metal Carbenoids. Intermolecular Formation of Azomethine Ylide from Methyl 2-Diazo-2-phenylacetate and Schiff Base: Intramolecular 1,3-Dipolar Cycloaddition

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Russian Journal of Organic Chemistry, Vol. 41, Iss. 6, 2005-06 ,pp. : 922-932

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Synthesis of a Novel Dispiroheterocyclic Framework via the Regioselective 1,3-Dipolar Cycloaddition Reaction of Azomethine Ylides

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