Synthesis of aryl perfluoroalkyl sulfides from aromatic disulfides
…, SA Kashtanov, VA Potemkin, JS Thrasher…
Index: Sipyagin; Enshov; Kashtanov; Potemkin; Thrasher; Waterfeld Russian Chemical Bulletin, 2004 , vol. 53, # 2 p. 420 - 434
Full Text: HTML
Citation Number: 4
Abstract
Abstract Thermolysis of xenon (ii) bis (perfluoroalkanecarboxylates) in the presence of diaryl disulfides occurs through the S—S bond cleavage to form dihalo-, halonitro-, and halodinitrophenyl perfluoroalkyl sulfides. The latter type of compounds was obtained for the first time. The main side process is the perfluoroalkylation of the aromatic ring.
Related Articles:
[Zhu, Rui-Heng; Shi, Xiao-Xin Synthetic Communications, 2012 , vol. 42, # 8 p. 1108 - 1114]