Iodine-catalyzed thioallylation of indoles using Bunte salts prepared from Baylis-Hillman bromides

Metal-free iodine-catalyzed regioselective thioallylation of indoles has been accomplished at room temperature using Bunte salts prepared from Baylis-Hillman bromides. The resulting multi-functional C3 thioallylated indoles exhibit ample structural diversity and good functional group tolerance.

Automated summary

Metal-free iodine-catalyzed regioselective thioallylation of indoles has been achieved at room temperature using Bunte salts prepared from Baylis-Hillman bromides. The resulting multi-functional C3 thioallylated indoles exhibit ample structural diversity and good functional group tolerance.