光激发
杠杆(统计)
化学
纳米技术
计算机科学
领域(数学)
分子轨道
生化工程
电子流
文艺复兴
基石
组合化学
作者
Muzi Li,Yuan-Zheng Cheng,Siqi You
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-03-20
卷期号:12 (12): eaed5284-eaed5284
被引量:1
标识
DOI:10.1126/sciadv.aed5284
摘要
Dearomatization reactions stand as a cornerstone strategy for constructing pharmacologically pivotal saturated rings. Photoexcitation reshapes the electron distribution within the frontier molecular orbitals of aromatics, thereby unlocking dearomatization pathways inaccessible in the ground state and furnishing structurally distinct molecular motifs. Contemporary synthetic methodologies leverage three discrete mechanistic paradigms to achieve this electronic activation: direct excitation, energy-transfer photocatalysis, and exciplex formation. These precisely tuned energy-delivery modes enable the dearomatization of a diverse array of (hetero)arenes, including highly robust substrates such as naphthalenes and benzenes, under mild reaction conditions. This review spotlights recent representative advances in these excited-state transformations. We envision that this synopsis will fuel ongoing innovation in the burgeoning field of photochemical dearomatization.
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