Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074, Aachen, Germany.
University of Jyvaskyla, Department of Chemistry, FI-40014, Jyväskylä, Finland.
Chem Asian J. 2022 Oct 4;17(19):e202200828. doi: 10.1002/asia.202200828. Epub 2022 Aug 29.
Treatment of N-methyl-S,S-diaryl sulfoximines with methyl trifluoromethanesulfonate provides bench-stable sulfoxinium salts in excellent yields. Applying them in Sonogashira-, Heck- and Suzuki-type cross-coupling reactions leads to the corresponding products by sequential C-S bond cleavage and C-C bond formation. Electronic factors induced by substituents on the S-aryl groups govern the coupling efficiency.
用三氟甲磺酸甲酯处理 N-甲基-S,S-二芳基磺亚胺可以得到在实验台上稳定的磺亚铵盐,产率优异。将它们应用于 Sonogashira、Heck 和 Suzuki 型交叉偶联反应中,通过顺序的 C-S 键断裂和 C-C 键形成,可以得到相应的产物。S-芳基取代基诱导的电子因素控制着偶联效率。