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α-Fluorination of Nitrobenzenes and Nitropyridines via Vicarious Nucleophilic Substitution of Hydrogen
Synlett ( IF 2 ) Pub Date : 2020-03-27 , DOI: 10.1055/s-0039-1690862
Michael F. Greaney 1 , Fayez Y. Al-Mkhaizim
Affiliation  

A highly selective C–H functionalization of nitrobenzenes and nitropyridines is reported using tandem vicarious nucleophilic substitution (VNS) chemistry with electrophilic fluorination using Selectfluor®. The process generates tertiary benzylic fluorides in good yield under simple, mild conditions and short reaction times.

中文翻译:

通过氢的替代亲核取代对硝基苯和硝基吡啶进行α-氟化

据报道,硝基苯和硝基吡啶的高选择性 C-H 官能化使用串联替代亲核取代 (VNS) 化学与使用 Selectfluor 的亲电氟化。该方法在简单、温和的条件和较短的反应时间内以良好的收率生成叔苄基氟化物。
更新日期:2020-03-27
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