Bodanszky M, Fagan D T
Int J Pept Protein Res. 1977 Nov;10(5):375-9. doi: 10.1111/j.1399-3011.1977.tb02810.x.
The imidazole catalyzed transesterification of active esters was used for the formation of the ester bond between the carboxyl group of protected amino acids and the hydroxyl group of a polymeric support applied in solid phase peptide synthesis. Anchoring of the C-terminal residue to the hydroxymethyl polymer proceeded smoothyl and provided a high degree of incorporation. No racemization was observed in the imidazole-catalyzed alcholysis. The procedure could be carried out with various active esters such as esters of o-and p-nitrophenol, 2,4,5-trichlorophenol, pentachlorophenol and N-hydroxysuccinimide.
咪唑催化的活性酯的酯交换反应被用于在固相肽合成中,在受保护氨基酸的羧基与聚合物载体的羟基之间形成酯键。C末端残基与羟甲基聚合物的锚定过程顺利进行,并实现了高掺入率。在咪唑催化的醇解反应中未观察到消旋化现象。该方法可使用各种活性酯来进行,如邻硝基苯酚酯、对硝基苯酚酯、2,4,5-三氯苯酚酯、五氯苯酚酯和N-羟基琥珀酰亚胺酯。