化学
双功能
自催化
电子受体
接受者
酮
光化学
辐照
电子供体
组合化学
有机化学
催化作用
凝聚态物理
物理
核物理学
作者
Cheng-Lin Chan,Yong‐Ting Tsao,Aira Shayne Paculba,Pei-Shan Lin,Zong‐Nan Tsai,Hsien‐Yi Chiu,Risa Kunitake,Ming-Jia Chiu,C. H. Yeh,Cheng‐chau Chiu,Hsuan‐Hung Liao
出处
期刊:Organic Letters
[American Chemical Society]
日期:2025-08-25
卷期号:27 (35): 9593-9598
被引量:3
标识
DOI:10.1021/acs.orglett.5c02448
摘要
We disclose an autocatalytic electron donor-acceptor (EDA) strategy by reutilizing redox auxiliary byproducts as in situ acceptors, enabling an external initiator-free activation of pro-aromatic dihydroquinazolinones (DHQZs). Spectroscopic and DFT data support the Lewis acid-enhanced aggregate formation where DHQZ serves as both donor and latent acceptor through its quinazolinone byproduct. Kinetic studies reveal a kinetic profile specifically representing autoinductive autocatalysis. This platform enables Giese-type acylation/alkylation, desulfonylation, and Minisci reactions, forging C-C, C-N, C-S, and C-Se bonds under mild conditions.
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