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Indole alkaloids Reissert synthesis

The chemistry of Reissert compounds has been the subject of numerous general reviews (3-10). In 1973 Popp gave a summary on the use of Reissert compounds in the synthesis of isoquinoline alkaloids and related compounds (7). We now wish to summarize new results that have appeared from 1973 to the end of 1985 for the application of Reissert compounds in the synthesis of isoquinoline as well as indole alkaloids. [Pg.2]

The formation of a Reissert anion (intermediate of type 16) is usually the introductory step in a great number of synthetic routes leading to isoquinoline as well as indole alkaloids and related compounds. On the one hand, the alkylation of a Reissert anion with alkyl halide followed by alkaline hydrolysis is the most frequently used method for the synthesis of 1-alkyl- or 1-arylalkylisoquinolines (20) (Scheme 4). On the other hand, Reissert anions react with aldehydes to form... [Pg.3]

Reissert synthesis of isoquinoline and indole alkaloids, 31,1 (1987) Reserpine, chemistry, 8, 287 (1965)... [Pg.266]

See other pages where Indole alkaloids Reissert synthesis is mentioned: [Pg.338]    [Pg.245]    [Pg.417]    [Pg.1]    [Pg.3]    [Pg.5]    [Pg.7]    [Pg.9]    [Pg.11]    [Pg.13]    [Pg.15]    [Pg.17]    [Pg.19]    [Pg.21]    [Pg.23]    [Pg.25]    [Pg.27]    [Pg.27]    [Pg.419]    [Pg.315]    [Pg.294]    [Pg.358]    [Pg.329]    [Pg.431]    [Pg.383]    [Pg.346]    [Pg.344]    [Pg.250]    [Pg.221]    [Pg.268]   
See also in sourсe #XX -- [ Pg.31 ]



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