Abstract
A novel and highly regioselective ammonium iodide-induced nonradical sulfenylation method for the construction of a C-S bond was developed via C-H functionalization. With DMSO or R1SO2NHNH2 as a sulfenylating agent, MeS- and R1S-substituted flavone derivatives were obtained in good yields. This method enriches current C-S bond formation chemistry, making it a highly valuable and practical method in pharmaceutical industry.
Original language | English |
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Pages (from-to) | 9167-9175 |
Number of pages | 9 |
Journal | Journal of Organic Chemistry |
Volume | 80 |
Issue number | 18 |
DOIs | |
State | Published - Sep 18 2015 |