Conclusions
The radical arylation of S-allylisothiuronium chloride at the double bond is accompanied by fragmentation leading to the formation of allylarenes and, depending on the catalyst used, formamidine disulfide or arylisothiuronium compounds.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 957–959, April, 1989.
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Yashkina, L.V., Kopylova, B.V. Radical arylation of S-allylisothiuronium chloride. Russ Chem Bull 38, 863–865 (1989). https://doi.org/10.1007/BF00953309
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DOI: https://doi.org/10.1007/BF00953309