化学
卡宾
立体选择性
炔烃
催化作用
钯
基质(水族馆)
组合化学
功能群
有机化学
海洋学
地质学
聚合物
作者
Ying Huang,Xin-Han Wang,Chun-Lin Zhang,Song Ye
出处
期刊:Organic Letters
[American Chemical Society]
日期:2024-04-16
卷期号:26 (16): 3441-3446
被引量:2
标识
DOI:10.1021/acs.orglett.4c00875
摘要
Herein, a cooperative N-heterocyclic carbene- and palladium-catalyzed three-component reaction of alkynes with aldehydes and fluoroalkyl iodides is developed. A series of biologically valuable CF2R-incorporated α-substituted enones was obtained in moderate to good yields. This mild catalytic method exhibits exclusive regio- and stereoselectivity, excellent functional group tolerance, and a broad substrate scope including terminal and internal alkynes. Mechanistic investigations disclose that this alkyne fluoroalkylacylation proceeds via a radical relay process in which vinyl iodides serve as putative reaction intermediates.
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