Literature DB >> 8045681

Preparation of an aspartic acid-containing protected peptide. Alternatives for overcoming a side reaction during HF treatment.

J Robles1, E Pedroso, A Grandas.   

Abstract

Treatment of the peptide-resin Ac-Asn-Ser(Bzl)-Gly-Asp(OFm)-pMeBHA with HF/anisole cleaves the peptide-resin bond and removes the benzyl group, as expected, but also yields an impurity (ca. 25%) in which the benzyl group is linked to the fluorenylmethyl protecting group. Separation of the desired peptide from the impurity can be accomplished by reversed-phase medium-pressure liquid chromatography. The side reaction does not take place when the gamma-carboxyl of aspartic acid is protected with the 2-(4-acetyl-2-nitrophenyl)ethyl group.

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Year:  1994        PMID: 8045681

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


  1 in total

1.  Solid-phase synthesis of a nucleopeptide from the linking site of adenovirus-2 nucleoprotein, -Ser(p5'CATCAT)-Gly-Asp-. Convergent versus stepwise strategy.

Authors:  J Robles; E Pedroso; A Grandas
Journal:  Nucleic Acids Res       Date:  1995-10-25       Impact factor: 16.971

  1 in total

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