1980International journal of peptide & protein researchRequires access

RACEMIZATION IN PEPTIDE SYNTHESIS

N. Leo Benoiton, Keiji Kuroda, FRANCIS M.F. CHEN

Open publisher page 15 citations

Abstract

A laboratory experiment involving the coupling of N-benzoylamino acids with methyl N epsilon-benzyloxycarbonyl-L-lysinate using various methods is described. The extents of racemization are determined by analysis for the protected diastereomeric dipeptide ester products by quantitation of the separated ester methyl proton peaks of their nuclear magnetic resonance (60 MHz) spectra. Synthesis of the starting materials and additional exercises are included as options.

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What this paper is about

A laboratory experiment involving the coupling of N-benzoylamino acids with methyl N epsilon-benzyloxycarbonyl-L-lysinate using various methods is described. The extents of racemization are determined by analysis for the protected diastereomeric dipeptide ester products by quantitation of the separated ester methyl proton peaks of their nuclear magnetic resonance (60 MHz) spectra. Synthesis of the starting materials and additional exercises are included as options.

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OpenAlex reports 15 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

A laboratory experiment involving the coupling of N-benzoylamino acids with methyl N epsilon-benzyloxycarbonyl-L-lysinate using various methods is described. The extents of racemization are determined by analysis for the protected diastereomeric dipeptide ester products by quantitation of the separated ester methyl proton peaks of their nuclear magnetic resonance (60 MHz) spectra. Synthesis of the starting materials and additional exercises are included as options.

Key concepts: Racemization, Peptide, Peptide synthesis, Chemistry, Stereochemistry, Biochemistry

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