Literature DB >> 604286

Active esters in the formation of ester bonds between amino acids and polymeric supports.

M Bodanszky, D T Fagan.   

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.

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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


  1 in total

1.  Mechanisms and prevention of trifluoroacetylation in solid-phase peptide synthesis.

Authors:  S B Kent; A R Mitchell; M Engelhard; R B Merrifield
Journal:  Proc Natl Acad Sci U S A       Date:  1979-05       Impact factor: 11.205

  1 in total

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