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环丁烷稠合四环骨架的构建:底物依赖的通过亲核环化实现的苯并呋喃(苯并噻吩)/马来酰亚胺的去芳构化[2+2]环加成反应

Construction of cyclobutane-fused tetracyclic skeletons substrate-dependent EnT-enabled dearomative [2+2] cycloaddition of benzofurans (benzothiophenes)/maleimides.

作者信息

Liao Zhi-Yu, Gao Fan, Ye Yu-Hang, Yu Qian-Hui, Yang Cui, Luo Qing-Yu, Du Fei, Pan Bin, Zhong Wen-Wu, Liang Wu

机构信息

College of Pharmacy, Chongqing Medical University, Chongqing, 400016, China.

College of Pharmacy, Third Military Medical University, Shapingba, Chongqing 400038, China.

出版信息

Chem Commun (Camb). 2024 Apr 18;60(33):4455-4458. doi: 10.1039/d4cc00690a.

Abstract

Herein, a novel and facile organic photosensitizer (thioxanthone)-mediated energy-transfer-enabled (EnT-enabled) dearomative [2+2] cycloaddition of aromatic heterocycles/maleimides for green synthesis of cyclobutane-fused polycyclic skeletons is reported. Mechanistic investigations revealed that different EnT pathways by triplet thioxanthone were initiated when different aromatic heterocycles participated in the reaction, giving the corresponding excited intermediates, which underwent the subsequent intermolecular [2+2] cycloaddition to access the desired highly functionalized cyclobutane-fused polycyclic skeletons.

摘要

在此,报道了一种新型且简便的有机光敏剂(噻吨酮)介导的、通过能量转移实现的(EnT介导的)芳香杂环/马来酰亚胺的脱芳构化[2+2]环加成反应,用于绿色合成稠合环丁烷的多环骨架。机理研究表明,当不同的芳香杂环参与反应时,三线态噻吨酮会引发不同的能量转移途径,生成相应的激发态中间体,这些中间体随后进行分子间[2+2]环加成反应,从而得到所需的高度官能化的稠合环丁烷多环骨架。

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