Metal-Free Difluoromethylthiolation, Trifluoromethylthiolation, and Perfluoroalkylthiolation with Sodium Difluoromethane- sulfinate, Sodium Trifluoromethanesulfinate or Sodium Perfluoro- alkanesulfinate
A method for direct difluoromethylthiolation of Ar−H bonds is introduced. The stable and easy-to-handle HCF2SO2Na is reduced with (EtO)2P(O)H in the presence of TMSCl to generate HCF2S+ for the regioselective difluoromethylthiolation of aromatic compounds including indoles, pyrroles, and activated benzenes. This method is also applicable for the trifluoromethylthiolation with CF3SO2Na and the perf
介绍了一种直接的二氟甲硫基化Ar-H键的方法。在TMSCl存在下,用(EtO)2 P(O)H还原稳定易处理的HCF 2 SO 2 Na ,生成HCF 2 S +,用于芳香族化合物(包括吲哚,吡咯和活化)的区域选择性二氟甲基硫醇化反应苯。该方法也适用于用芳烃和杂芳烃用CF 3 SO 2 Na进行三氟甲基硫醇化和用R f SO 2 Na进行全氟烷基硫醇化。还讨论了与无金属亲电性氟代烷基硫基化反应相关的反应机理。
Haloalkylthio, -sulfinyl and -sulfonyl arylpyrrole insecticidal, acaricidal and fungicidal agents