化学
对映选择合成
铱
碘化物
催化作用
激进的
光化学
氧化还原
药物化学
有机化学
作者
Eric Meggers,Haohua Huo,Xiaoqiang Huang,Xiaodong Shen,Klaus Harms
出处
期刊:Synlett
[Thieme Medical Publishers (Germany)]
日期:2015-12-23
卷期号:27 (05): 749-753
被引量:43
标识
DOI:10.1055/s-0035-1561284
摘要
A visible-light-activated enantioselective radical perfluoroalkylation of 2-acyl imidazoles with perfluoroalkyl iodides (CF3I, C3F7I, C4F9I, C6F13I, C8F17I and C10F21I) and perfluorobenzyl iodide at the α-position of the carbonyl group is reported. Enantioselectivities with up to >99.5% ee are achieved. The process uses a dual-function chiral Lewis acid/photoredox catalyst at loadings of 2–4 mol% and constitutes a redox-neutral, electron-catalyzed reaction that proceeds via intermediate perfluoroalkyl radicals.
科研通智能强力驱动
Strongly Powered by AbleSci AI