Issue 16, 1982

Improved deprotection in solid phase peptide synthesis: deprotection of Ni-formyl-tryptophan to tryptophan in low concentrations of HF in Me2S–p- thiocresol mixtures

Abstract

The Ni-formy protecting group of tryptophan in solid phase peptide synthesis was found to be removed efficiently and quantitatively by a new reagent, HF–Me2S–p-thiocresol–p-cresol (25: 65: 5: 5, v/v/v/v) without detectable side reaction.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1982, 896-897

Improved deprotection in solid phase peptide synthesis: deprotection of Ni-formyl-tryptophan to tryptophan in low concentrations of HF in Me2S–p- thiocresol mixtures

W. F. Heath, J. P. Tam and R. B. Merrifield, J. Chem. Soc., Chem. Commun., 1982, 896 DOI: 10.1039/C39820000896

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