The disulphide linkage of the antiviral antibiotic acetylaranotin is shown to be highly reactive, undergoing novel insertion reactions with elemental sulphur and hydrogen cyanide and cleavage reactions with hydrogen sulphide and dimethyl disulphide.
K. C. Murdock and R. B. Angier, J. Chem. Soc. D, 1970, 55 DOI: 10.1039/C29700000055
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