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Iron-catalyzed benzylic addition of 2-methyl azaarenes to substituted trifluoromethyl ketones
Synthetic Communications ( IF 1.8 ) Pub Date : 2021-01-05 , DOI: 10.1080/00397911.2020.1867178
Jiayu Alicia Lim 1 , Yong-Chua Teo 1
Affiliation  

Abstract

This paper demonstrated a new and economical methodology using Fe(ClO4)2·H2O as a catalyst for the direct C(sp3)–H functionalization of 2-methyl azaarenes via addition to trifluoromethyl ketones. The use of Fe salts as a Lewis acid catalyst has shown great potential as an accessible, affordable, and effective catalyst for the reaction. Under mild, optimized conditions, an extensive range of 2-alkenylated azaarenes was produced with yields of up to 95%.



中文翻译:

铁催化的2-甲基氮杂芳烃苄基加成到取代的三氟甲基酮上

抽象的

本文展示了一种新的经济的方法,使用Fe(ClO 42 ·H 2 O作为催化剂,通过添加三氟甲基酮将2-甲基氮杂芳烃直接进行C(sp 3)-H官能化。铁盐作为路易斯酸催化剂的使用已显示出巨大的潜力,可作为一种容易获得,负担得起且有效的反应催化剂。在温和,优化的条件下,生产了范围广泛的2-烯基氮杂氮杂芳烃,收率高达95%。

更新日期:2021-03-08
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