Vyacheslav Diev - An efficient and stereoselective cycloaddition of C-aryl and C-amido nitrones to dimethyl 2-benzylidenecyclopropane-1,1-dicarboxylate

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      Publication Details (including relevant citation   information):

      Tetrahedron    2011, 67, 2391-2395

      Abstract:

      1,3-Dipolar cycloadditions of dimethyl   2-benzylidenecyclopropane-1,1-dicarboxylate and a number of   C-aryl or C-amido nitrones proceed with high   efficiency and selectivity with the formation of only one   isomeric spiro[cyclopropane-1,4-isoxazolidine]   cycloadduct.

      Address (URL): http://www.sciencedirect.com/science/article/pii/S004040201100192X