Novel conversion of thiols into disulfides, via S-nitrosothiol intermediates using trichloronitromethane

1999-10-15
Demir, Ayhan Sıtkı
Igdir, AC
Mahasneh, AS
An efficient oxidative coupling of thiols to give disulfides via thionitrite (S-nitrosothiol) intermediate is described using trichloronitromethane as an efficient reagent in organic solvents and water. Cysteine and glutathione are converted into the corresponding disulfides in water in high yields.

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Citation Formats
A. S. Demir, A. Igdir, and A. Mahasneh, “Novel conversion of thiols into disulfides, via S-nitrosothiol intermediates using trichloronitromethane,” TETRAHEDRON, pp. 12399–12404, 1999, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/56550.