An odorless, one-pot synthesis of nitroaryl thioethers via S<sub>N</sub>Ar reactions through the in situ generation of S-alkylisothiouronium salts
作者:Guo-ping Lu、Chun Cai
DOI:10.1039/c4ra11490f
日期:——
A newly developed C–S bond formation nucleophilic aromatic substitution (SNAr) reaction in aqueous Triton X-100 (TX100) micelles has been disclosed. This chemistry, in which odorless, cheap and stable thiourea in place of thiols is used as the sulfur reagent, provides an efficient approach for the generation of nitroaryl thioethers, which are useful structural units of many bioactive molecules, rendering
新开发的C-S键的形成亲核芳香取代(S Ñ在含水的Triton X-100(TX100)胶束的Ar)反应已经公开。该化学方法使用无味,廉价且稳定的硫脲代替硫醇作为硫试剂,为产生硝基芳基硫醚提供了一种有效的方法,硝基芳基硫醚是许多生物活性分子的有用结构单元,使该方法对于两种合成方法都具有吸引力和药物化学。