可见光诱导吖啶催化的n -杂环选择性脱烷基反应

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Chemical Communications Pub Date : 2025-04-23 Epub Date: 2025-04-08 DOI:10.1039/d5cc00609k
Shanshan Liu , Yaoyao Zhang , Xianying Zhou , Lin-Yu Jiao
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引用次数: 0

摘要

我们开发了一种有效的、通用的策略,通过吖啶光催化电子转移和氢原子转移来促进氮杂环的n -脱烷基反应。这种方法有效地避免了对过渡金属催化的需要,并且突出了广泛的底物范围以及独特的化学选择性。值得注意的是,该方法允许脱保护特权但稳定的n -烷基,从而填补了n -杂芳烃实际n -脱烷基的空白。
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Visible-light-induced acridinium-catalyzed selective N-dealkylation of N-heterocycles†
We have developed an efficient and general strategy for N-chlorosuccinimide (NCS)-promoted N-dealkylation of aza-heterocycles via acridinium-photocatalyzed electron transfer and hydrogen atom transfer. This approach effectively obviates the need for transition metal catalysis and features wide substrate scope as well as exclusive chemo-selectivity. Remarkably, the method allowed the deprotection of the privileged but stable N-alkyl group, thus filling a gap in the practical N-dealkylation of N-heteroaromatics.
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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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