Electrochemical regioselective methylthiolation of imidazo[2,1-<i>b</i>]thiazoles with DMSO
With DMSO both as the source of -SMe unit and solvent, an efficient and green electrochemical methylthiolation reaction of imidazo[2,1-<i>b</i>]thiazoles was developed. The transformation was performed at room temperature in 8 h under external transition metal- and oxidant-free condition. Moreover, the 2,3-dihydroimidazo[2,1-<i>b</i>]thiazoles and 2-phenylbenzo[d]imidazo[2,1-<i>b</i>]thiazole also proceeded smoothly. This strategy provides C-5 methylthiolation products with broad scope in 73–91% yields.
Publication Details
- Journal
- Figshare
- Published
- 2025-01-01
- DOI
- https://doi.org/10.6084/m9.figshare.28247876
- Primary Topic
- Sulfur-Based Synthesis Techniques
- Type
- article
- Field-Weighted Citation Impact
- 0.00