化学
催化作用
磺酰
镍
卤化物
有机化学
药物化学
高分子化学
烷基
作者
Jianquan Hong,Xiaoyu Wang,Kui Zhao,Xifei Chen,Ruilong Feng,Chunxiang Li,Chongbin Wei,Xinxin Gong,Feng Zheng,Changge Zheng
出处
期刊:Organic Letters
[American Chemical Society]
日期:2024-11-08
卷期号:26 (46): 9967-9972
被引量:2
标识
DOI:10.1021/acs.orglett.4c03820
摘要
An efficient nickel-catalyzed direct fluorosulfonylation of vinyl bromides and benzyl bromides under mild reaction conditions has been developed for sulfonyl fluorides utilizing Na2S2O4 and NFSI as the sulfur dioxide and fluorine sources, respectively. This reaction system tolerates organic bromide compounds, such as β-styryl bromides, alkyl vinyl bromides, and benzyl bromides, to achieve corresponding sulfonyl fluorides in moderate to good yields, with convenient operation, mild conditions, broad substrate scope, good functional group compatibility, and excellent retention of configuration to vinyl bromides.
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