| Literature DB >> 604286 |
Abstract
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.Entities:
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Year: 1977 PMID: 604286 DOI: 10.1111/j.1399-3011.1977.tb02810.x
Source DB: PubMed Journal: Int J Pept Protein Res ISSN: 0367-8377