Silyl compound 1 reacts with iodobenzene diacetate in the presence of trifluoromethanesulfonic acid to give hypervalent iodine compound 2. Treatment of compound 2 with tetrabutylammonium fluoride at room temperature generates benzyne 3, which in turn give several types of cyclic compounds in the presence of a trapping agent such as furan.1) Since the generation of 3 from 1 is carried out under mild conditions, this methodology can be utilized in various fields.
The reaction of 1 with 1,2-bis(trichlorotelluro)benzene can also provide telluranthene 4.2)
Maintenance Notice (3:30 AM July 12 - 4:00 AM July 14, 2025): This website is scheduled to be unavailable due to maintenance. Maintenance may be completed earlier than scheduled. We appreciate your patience and understanding.
Published TCIMAIL newest issue No.198