Journal of the Chemical Society. Chemical communications p. 834 - 835 (1983)
Update date:2022-08-15
Topics:
Fishwick, Brian R.
Rowles, David K.
Stirling, Charles J. M.
Thiolate ions react with bromonitromethane to give nitronate ion and, initially, sulphenyl bromide which reacts with further thiolate ion to give disulphide; when the disulphide bears an appropriately placed nitrile function, intramolecular attack by the nitronate ion at this function and subsequent intramolecular displacement of thiolate ion yields aminothiophenes.
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