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Triphenylphosphite, reaction+carbonyls

In other words, the aromatic carboxylic acid is activated by the pyridinyl triphosphonate cation so that the weakly basic aromatic amine can effectively attack the carbonyl center. The reaction has not been utilized commercially because the costs of recovering and regenerating triphenylphosphite far outweigh the cost advantage of using unmodified diacids. [Pg.993]


See other pages where Triphenylphosphite, reaction+carbonyls is mentioned: [Pg.347]    [Pg.112]    [Pg.297]    [Pg.396]    [Pg.438]    [Pg.338]    [Pg.219]    [Pg.237]    [Pg.438]    [Pg.101]   
See also in sourсe #XX -- [ Pg.30 , Pg.34 , Pg.36 , Pg.37 ]




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Triphenylphosphites

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