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Deoxygenative 1,1‐Bis‐trifluoromethylthiolation of Aromatic Aldehydes to Access Bis(trifluoromethylthio)methylarenes
Advanced Synthesis & Catalysis ( IF 5.4 ) Pub Date : 2020-09-17 , DOI: 10.1002/adsc.202000861
Yin‐Li Liu 1 , Xiu‐Hua Xu 1 , Feng‐Ling Qing 1
Affiliation  

A deoxygenative 1,1‐bis‐trifluoromethylthiolation of readily available aromatic aldehydes with AgSCF3 in the presence of KI and (NH4)2SO4 was established. This reaction delivered a series of bis(trifluoromethylthio)methylarenes in moderate to high yields. The precise control of the generation and decomposition of SCF3 anion is the key to the successful transformation.

中文翻译:

芳香醛的脱氧1,1-双-三氟甲基硫醇化反应制得双(三氟甲硫基)甲基芳烃

在KI和(NH 42 SO 4存在下,用AgSCF 3对易得的芳族醛进行了脱氧1,1-双-三氟甲基硫醇化反应。该反应以中等至高产率递送了一系列双(三氟甲硫基)甲基芳烃。精确控制SCF 3阴离子的生成和分解是成功转化的关键。
更新日期:2020-11-19
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