Issue 8, 1977

Novel reaction of cysteine with phenolic amino-acids in hydrobromic acid: reversible formation of 3-cystein-S-yltyrosine and cystein-S-yldopas

Abstract

Cystine reacts reversibly with tyrosine and dopa in hydrobromic acid to give 3-cystein-S-yltyrosine (6) and cystein-S-yldopas (3)–(5) in an electrophilic reaction involving HO2CCH(NH2)CH2S+, the sulphenyl ion from cysteine.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1977, 251-252

Novel reaction of cysteine with phenolic amino-acids in hydrobromic acid: reversible formation of 3-cystein-S-yltyrosine and cystein-S-yldopas

S. Ito and G. Prota, J. Chem. Soc., Chem. Commun., 1977, 251 DOI: 10.1039/C39770000251

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