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Pyridinium betaines acid esters

In another example of heterocyclic ring synthesis, pyridinium salts 816 require only Et3N for deprotonation, the resulting ylides 817 add to esters of 2-bromo-2-alkenecarboxylic acids or analogous benzonitriles to give intermediate betaines 818 which, via intramolecular nucleophilic attack, give indolizines 819 (Scheme 174) <1999JOC7618>. [Pg.598]


See other pages where Pyridinium betaines acid esters is mentioned: [Pg.1560]    [Pg.5337]    [Pg.5337]    [Pg.5337]    [Pg.100]    [Pg.84]    [Pg.126]    [Pg.126]    [Pg.51]    [Pg.588]    [Pg.37]    [Pg.184]    [Pg.126]    [Pg.262]   
See also in sourсe #XX -- [ Pg.17 ]




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