化学
三氟甲基化
催化作用
区域选择性
组合化学
有机化学
三氟甲基
烷基
作者
Km Sadhana,Sandeep Kumawat,Kishore Natte,K. Jyothi
出处
期刊:Synlett
[Thieme Medical Publishers (Germany)]
日期:2025-05-09
卷期号:36 (15): 2261-2266
被引量:3
标识
DOI:10.1055/s-0043-1775481
摘要
Abstract We present a general and scalable approach for the C(sp2)–H or S–H trifluoromethylation of arenes and heteroarenes. This method employs bench-stable CF3SO2Na as the CF3 source, with Ag2O serving as the catalyst and K2S2O8 as the oxidant. Notably, the protocol features broad functional-group compatibility, mild conditions, and high regioselectivity. Furthermore, it is applicable to biologically relevant molecules such as caffeine, pentoxifylline, ganciclovir triacetate, and mercaptopurine.
科研通智能强力驱动
Strongly Powered by AbleSci AI