Reactions of cysteine sulfenyl thiocyanate with thiols to give unsymmetrical disulfides
SL Alguindigue Nimmo, K Lemma…
Index: Alguindigue Nimmo, Susan L.; Lemma, Kelemu; Ashby, Michael T. Heteroatom Chemistry, 2007 , vol. 18, # 5 p. 467 - 471
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Citation Number: 14
Abstract
Abstract Cysteine sulfenyl thiocyanate (CSSCN) reacts with thiols at pH 0 to cleanly yield disulfides. 2-Mercaptoethanol (2-MESH), 3-mercaptopropionic acid (3-MPASH), penicillamine (PENSH), and glutathione (GSH) react with CSSCN to give the corresponding mixed disulfides: 2-MESSC, 3-MPASSC, PENSSC, and GSSC. These compounds are stable at pH 0 and have been characterized by 1 H and 13 C NMR spectroscopy.© 2007 Wiley ...
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[Purdie,J.W. Canadian Journal of Chemistry, 1969 , vol. 47, p. 1037 - 1043]