The direct α-Csp2£H functionalization and thiomethylation of α-oxoketene dithioacetals (DTAs) has been accomplished with dimethyl sulfoxide (DMSO) in the presence of iodine and a copper(I) salt for the first time. A prerequisite is the in situ iodination of the α-Csp2 atom of dithioacetals that could offer other reaction channels. The operationally simple one-pot protocol includes region-defined consecutive iodination and sulfenylation of the challenging α-Csp2£H bond of dithioacetals employing cheap and readily available reagents. DMSO here plays a dual role as thiomethyl source and solvent.
CITATION STYLE
Shukla, G., Srivastava, A., Nagaraju, A., Raghuvanshi, K., & Singh, M. S. (2015). Iodine-Mediated Copper-Catalyzed Efficient α-C(sp2)-Thiomethylation of α-Oxoketene Dithioacetals with Dimethyl Sulfoxide in One Pot. Advanced Synthesis and Catalysis, 357(18), 3969–3976. https://doi.org/10.1002/adsc.201500634
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