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• W2953131864 abstract "Treatment of nitroarenes having electron-withdrawing groups at the ortho or para position with alkanethiol in the presence of cesium carbonate in dimethyl sulfoxide at 25 °C leads to nucleophilic displacement of the nitro group with the alkylthio group. Cesium carbonate is superior to other bases such as potassium carbonate, sodium carbonate, and triethylamine. The cesium-mediated nucleophilic aromatic substitution reaction provides a mild yet powerful and user-friendly protocol for the synthesis of aryl sulfides." @default.
• W2953131864 created "2019-06-27" @default.
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• W2953131864 date "2006-03-01" @default.
• W2953131864 modified "2023-09-25" @default.
• W2953131864 title "Nucleophilic aromatic substitution reaction of nitroarenes with alkyl- or arylthio groups in dimethyl sulfoxide by means of cesium carbonate" @default.
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• W2953131864 doi "https://doi.org/10.1016/j.tet.2005.11.073" @default.
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