
Journal of Organic Chemistry p. 338 - 349 (2018)
Update date:2022-08-05
Topics:
Guo, Yu-Jing
Lu, Shuai
Tian, Lu-Lu
Huang, En-Ling
Hao, Xin-Qi
Zhu, Xinju
Shao, Tian
Song, Mao-Ping
Novel iodine-induced sulfonylation and sulfenylation of imidazopyridines have been described using sodium sulfinates as the sulfur source. This strategy enables highly selective difunctionalization of imidazo[1,2-a]pyridine to access sulfones and sulfides in good yields. A wide range of substrates and functional groups were well-tolerated under optimized conditions. Moreover, control experiments have been conducted, indicating a radical pathway involved in the reaction mechanisms.
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