化学
亲核芳香族取代
硝基苯
芳基
硝基
药物化学
硫化物
二硫键
硝基化合物
极性效应
亲核取代
有机化学
催化作用
烷基
生物化学
作者
Naoki Enjo,Rong Lü,Tetsuo Miyakoshi
标识
DOI:10.2174/157017941006140206105221
摘要
A series of sulfides was successfully synthesized from nitroarenes by SNAr reaction via elimination of a nitro or phenylsulfonyl group. The SNAr reaction mechanism is found to depend on the position and type of substituents, and the effect of two-electron withdrawing groups was also examined. Keywords: Sulfide, SNAr reaction, nitro group, aryl disulfide.
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