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Isoureas carboxylic acid esters

Figure 3.1 EDC reacts with carboxylic acids to create an active-ester intermediate. In the presence of an amine nucleophile, an amide bond is formed with release of an isourea by-product. Figure 3.1 EDC reacts with carboxylic acids to create an active-ester intermediate. In the presence of an amine nucleophile, an amide bond is formed with release of an isourea by-product.
Another in situ procedure for activating carboxylic acids utilizes earbodiimides, such as dicyclohexylcarbodiimide (DCC). DCC (19) plays an important role in peptide synthesis. Addition of a carboxylic acid to the C-N double bond leads to the activated species, an acyl isourea 20, which upon attack by a nucleophile (and alcohol or an amine) releases the corresponding ester or amide along with 21 (for the mechanism, see Chapter 5). However, in the conversion of 5 to 7 the DCC procedure gives poor results. [Pg.128]

All other carboxylic acid derivatives in Table 6.1, in which the leaving group is bound to the carboxyl carbon through an O atom, are increasingly better acylating agents than carboxylic acid alkyl esters (entry 3) in the order carboxylic acid phenyl ester (entry 4) < acyl isourea (entry 7) < mixed carboxylic acid/carbonic acid anhydride (entry 8) < carboxylic acid anhydride (entry 9) < mixed carboxylic acid anhydride (entry 10). [Pg.268]

RCO2H, R OH, DCC/DMAP, EtjO, 25°C, l-24h, 70-95% yield. This method is suitable for a large variety of hindered and unhindered acids and alcohols. The use of Sc(OTf)3 as a cocatalyst improves the esterification of 3° alcohols. Carboxylic acids that can form ketenes with DCC react preferentially with aliphatic alcohols in the presence of phenols whereas those that do not show the opposite selectivity. In some sterically congested situations the 0-acyl urea will migrate to an unreactive A-acyl urea in competition with esterification. Carbodi-imide I was developed to make the urea by-product water soluble and thus easily washed out. Isoureas are prepared from a carbodiimide and an alcohol which upon reaction with a carboxylic acid give esters in excellent yield. A polymer supported version of this process has been developed. This process has been reviewed. Note that DCC is a potent skin irritant in some individuals. [Pg.539]


See other pages where Isoureas carboxylic acid esters is mentioned: [Pg.699]    [Pg.216]    [Pg.75]    [Pg.190]    [Pg.279]    [Pg.243]    [Pg.90]    [Pg.146]    [Pg.170]    [Pg.773]    [Pg.774]    [Pg.774]    [Pg.94]    [Pg.189]   
See also in sourсe #XX -- [ Pg.22 , Pg.181 ]




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