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Investigation of the scope and mechanism of copper catalyzed regioselective methylthiolation of aryl halides Dedicated to Professor Dr. Irina Beletskaya

机译:铜对芳基卤化物的区域选择性甲基硫醇化反应的范围和机理的研究专门针对伊琳娜·贝莱茨卡娅教授

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摘要

Methylthiolation of structurally diverse aryl halides was accomplished under fluoride free conditions using catalytic amounts of CuI, and DMSO as the methylthiolation source. Optimization studies unveiled several varieties of promoters among which Zn(OAc)_2 was found ideal. The analogous reaction with DMSO-d_6 afforded corresponding deuterated aryl methyl thioether with 99% purity. Mechanistic studies revealed CuSMe as the active methylthiolation agent.
机译:使用催化量的CuI和DMSO作为甲基硫醇化来源,在无氟条件下完成结构多样的芳基卤化物的甲基硫醇化反应。优化研究揭示了几种启动子,其中Zn(OAc)_2被认为是理想的。与DMSO-d-6的类似反应得到相应的具有99%纯度的氘代芳基甲基硫醚。机理研究表明,CuSMe是活性的甲基硫醇化剂。

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