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O-Aminocarboxylic acid esters

Dihydro-5H-[l,3]oxazolo[2,3-b]quinazol-5-ones from o-aminocarboxylic acid esters and 2-balogenisocyanates... [Pg.103]

Polycondensation is easier with amino carboxylic esters, since the —COOR-group is less resonance-stabilized (cf. nylon 7 and nylon 11). Even less stable, and therefore very reactive, is the acyl chloride group. However, the acyl chloride of the a,o)-aminocarboxylic acids is not easy to handle (purify, etc.), and it is not easy to control polymer formation. [Pg.987]

Quinazolone-2-carboxylic acid esters from o-aminocarboxylic acid amides... [Pg.136]

Imidazoles from purines o-Aminocarboxylic acid amides from pyrimidine ring Carboxylic acid amides from hydroxamic acid benzyl esters... [Pg.19]

Sodium hydrogen carbonate a-Aminocarboxylic acid esters from aziridinones via their O-alkylation... [Pg.47]

See other pages where O-Aminocarboxylic acid esters is mentioned: [Pg.51]    [Pg.115]    [Pg.303]    [Pg.351]    [Pg.257]    [Pg.279]    [Pg.380]    [Pg.412]    [Pg.104]    [Pg.242]    [Pg.51]    [Pg.115]    [Pg.303]    [Pg.351]    [Pg.257]    [Pg.279]    [Pg.380]    [Pg.412]    [Pg.104]    [Pg.242]    [Pg.42]    [Pg.212]    [Pg.465]    [Pg.239]    [Pg.362]    [Pg.283]    [Pg.348]    [Pg.115]    [Pg.375]   


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Aminocarboxylate

Aminocarboxylic acids

O"- ester

O-Aminocarboxylic acids

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