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Aryl acidolytic cleavage

Figure 3.18. Acidolytic cleavage of aryl benzyl ethers as competing reaction during the acidolysis of N-benzylamides [212],... Figure 3.18. Acidolytic cleavage of aryl benzyl ethers as competing reaction during the acidolysis of N-benzylamides [212],...
Heterocycles containing an NH group, such as pyrroles, indoles, imidazoles, triazoles, etc., can be linked to insoluble supports as N-alkyl, N-aryl, or N-acyl derivatives (Table 3.29). The optimal choice depends mainly on the NH acidity of the heterocycle in question. Increasing acidity will facilitate the acidolytic cleavage of N-benzyl groups and the nucleophilic cleavage of /V-acyl groups from these heterocycles. [Pg.99]


See other pages where Aryl acidolytic cleavage is mentioned: [Pg.299]    [Pg.262]    [Pg.326]    [Pg.405]    [Pg.463]    [Pg.162]    [Pg.115]   
See also in sourсe #XX -- [ Pg.131 ]




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Acidolytic cleavage

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