Remote radical alkynylation of unactivated C(sp3)–H bonds of ethynesulfonamides†

IF 4.2 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Chemical Communications Pub Date : 2025-04-14 Epub Date: 2025-04-10 DOI:10.1039/d5cc01215e
Pan Zhou , Mengru Guo , Jiawei Li , Xu Li , Danyang Xie , Bo Qin , Yong Xia
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Abstract

We report an efficient protocol for the construction of δ-alkynyl amides via 1,5-hydrogen atom transfer and alkynyl group transfer of ethynesulfonamides. The readily installed ethynesulfonamides serve as both an amidyl radical precursor and an alkyne source. This reaction features excellent site selectivity for tertiary, secondary, primary, and benzylic C(sp3)–H bonds.

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乙基磺酰胺非活化C(sp3)−H键的远端自由基烷基化
我们报道了一种通过1,5-氢原子转移和乙烯磺酰胺炔基转移构建δ-炔基酰胺的高效方案。易安装的乙基磺酰胺既可作为酰胺基自由基前体,又可作为炔源。该反应对叔键、仲键、伯键和苯基C(sp3) -H键具有很好的选择性。
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来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
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