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Nonasymmetric transformations

Homogeneous Titanium-based Catalysts for Nonasymmetric Transformations... [Pg.103]

The alkylation of indoles, and indole derivatives unsubstituted at the C-3 position is troublesome (eq 6). While simple secondary amines are not efficient in catalyzing this nonasymmetric transformation, imidazoUdinone catalyst 1 allowed the preparation of the corresponding aldehyde albeit in modest yield (up to 38%). This in situ reductive amination provided rapid access to homotryptamines. ... [Pg.307]

See other pages where Nonasymmetric transformations is mentioned: [Pg.113]    [Pg.114]    [Pg.115]    [Pg.117]    [Pg.119]    [Pg.121]    [Pg.123]    [Pg.125]    [Pg.127]    [Pg.129]    [Pg.131]    [Pg.135]    [Pg.137]    [Pg.139]    [Pg.141]    [Pg.143]    [Pg.145]    [Pg.147]    [Pg.153]    [Pg.157]    [Pg.159]    [Pg.161]    [Pg.163]   


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Homogeneous Titanium-based Catalysts for Nonasymmetric Transformations

Nonasymmetric transformations homogeneous titanium-based

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