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Issue 24, 1987
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Use of esters of 2,5-diphenyl-2,3-dihydro-3-oxo-4-hydroxythiophene dioxide in solid phase peptide synthesis. A new procedure for attachment of the first amino acid

Abstract

The title esters derived from fluorenylmethoxycarbonyl amino acids undergo transesterification with hydroxymethyl polymers in the presence of tertiary base without racemisation.

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Article type: Paper
DOI: 10.1039/C39870001870
Citation: J. Chem. Soc., Chem. Commun., 1987,0, 1870-1871
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    Use of esters of 2,5-diphenyl-2,3-dihydro-3-oxo-4-hydroxythiophene dioxide in solid phase peptide synthesis. A new procedure for attachment of the first amino acid

    R. Kirstgen, R. C. Sheppard and W. Steglich, J. Chem. Soc., Chem. Commun., 1987, 0, 1870
    DOI: 10.1039/C39870001870

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