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Caiboxylic groups protection

Some examples for the introduction of amino protecting groups such as 2-(4-nitro-phenyl)ethoxycarbonyl (npeoc) or benzyloxycarbonyl (Z) were already given in the compilation of carbamates produced with imidazolium caiboxylates in Section 4.6.1. [Pg.139]

The phenyl group became a practical protective group for carboxylic acids when Sharpless published a mild, effective one-step method for its conversion to a carboxylic acid.1 It has recently been used in a synthesis of the amino acid statine, where it served as a masked or caiboxylic acid equivalent.2... [Pg.384]

Albericio F (2000) Orthogonal protecting groups for N -amino and C-terminal caiboxyl functions in solid-phase synthesis. Biopolymers (Peptide Sci) 55 123-139... [Pg.268]


See other pages where Caiboxylic groups protection is mentioned: [Pg.369]    [Pg.203]    [Pg.413]    [Pg.101]    [Pg.108]   


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