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Chemoselective nitrone formation

As anticipated from the chemistry of oxime and nitrone formation, we quickly fotmd that the amide formation was remarkably chemoselective. Carboxylic acids,... [Pg.19]

In all the above examples, the synthesis of nitronates (5) is rather chemose-lective. In any case, data on the formation of their structural isomers, viz, the corresponding nitrocyclopropanes (13), are lacking. However, the synthesis of five-membered nitronates (5) with the use of sulfur or selenium ylides is not chemoselective (see Scheme 3.16). [Pg.446]


See other pages where Chemoselective nitrone formation is mentioned: [Pg.380]    [Pg.380]    [Pg.211]    [Pg.308]    [Pg.398]    [Pg.1292]    [Pg.73]    [Pg.1292]   


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