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C-S coupling with nitro group as leaving group via simple inorganic salt catalysis
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作者 maojie xuan Chunlei Lu Bo-Lin Lin 《Chinese Chemical Letters》 SCIE CAS CSCD 2020年第1期84-90,共7页
An efficient and practical synthetic protocol to synthesize nonsymmetrical aryl thioethers by nucleophilic aromatic substitution(S_NAr)reaction of nitroarenes by thiols with potassium phosphate as the catalyst is desc... An efficient and practical synthetic protocol to synthesize nonsymmetrical aryl thioethers by nucleophilic aromatic substitution(S_NAr)reaction of nitroarenes by thiols with potassium phosphate as the catalyst is described.Various moderate to strong electron-withdrawing functional groups are tolerated by the system to provide thioethers in a good to excellent yields.We also showed that the present method allows access to 3 drug examples in a short reaction time.Finally,mechanistic studies suggest that the reaction may form the classic Meisenheimer complex through a two-step additionelimination mechanism. 展开更多
关键词 Inorganic-salt catalysis Nucleophilic aromatic substitution C-S bond Denitrification coupling Kinetic isotope effect Meisenheimer complex
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