Literature DB >> 429104

Facile thiolytic removal of the o-nitrophenylsulphenyl amino-protecting group.

M Stern, A Warshawsky, M Fridkin.   

Abstract

2-Mercaptopyridine was used to effect the selective, mild and efficient cleavage of the o-nitrophenylsulphenyl amino-protecting group from several amino acids and peptides. By utilization of this reagent a stepwise synthesis of the tetrapeptide Thr-Lys-Leu-Arg([Leu3]tuftsin) was successfully achieved. The potential use of 2-mercaptopyridine in mechanized peptide synthesis via the polymeric reagents approach is discussed.

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Year:  1979        PMID: 429104     DOI: 10.1111/j.1399-3011.1979.tb01885.x

Source DB:  PubMed          Journal:  Int J Pept Protein Res        ISSN: 0367-8377


  2 in total

Review 1.  Tuftsin, Thr-Lys-Pro-Arg. Anatomy of an immunologically active peptide.

Authors:  M Fridkin; P Gottlieb
Journal:  Mol Cell Biochem       Date:  1981-12-04       Impact factor: 3.396

2.  Solid-phase synthesis of an RNA nucleopeptide fragment from the nucleoprotein of poliovirus.

Authors:  C M Dreef-Tromp; H van den Elst; J E van den Boogaart; G A van der Marel; J H van Boom
Journal:  Nucleic Acids Res       Date:  1992-05-25       Impact factor: 16.971

  2 in total

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