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Glycine site antagonists, synthesis

When C3 is the only position open, the C3 electrophilic substitutions obviously occur exclusively. The following Vilsmeier-Haack reaction was applied to the synthesis of a novel class of glycine site antagonists of the ionotropic A -methyl-D-aspartate (NMDA) glutamatergic receptor. ... [Pg.33]

See other pages where Glycine site antagonists, synthesis is mentioned: [Pg.244]    [Pg.882]    [Pg.400]    [Pg.252]    [Pg.170]    [Pg.171]    [Pg.172]    [Pg.175]    [Pg.252]    [Pg.183]   
See also in sourсe #XX -- [ Pg.33 ]



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Glycine synthesis

Synthesis sites

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