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Iminoester 1 + 2 -type

While virtually all of the research described above has focused on the inter-molecular cycloaddition of azomethine ylides, the intramolecular process holds considerable promise for the synthesis of polycyclic natural products. The Pfaltz group reported an intramolecular catalytic asymmetric cyclization of aryl iminoesters 112 using a complex of silver acetate with PHOX type ligand 100 (Scheme 2.29,... [Pg.63]

See other pages where Iminoester 1 + 2 -type is mentioned: [Pg.168]    [Pg.28]    [Pg.48]    [Pg.49]    [Pg.181]    [Pg.462]    [Pg.193]    [Pg.729]    [Pg.16]    [Pg.16]    [Pg.294]    [Pg.27]    [Pg.407]    [Pg.168]   


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Iminoester

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