Issue 33, 2024

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

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.

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

Supplementary files

Article information

Article type
Communication
Submitted
16 Feb 2024
Accepted
21 Mar 2024
First published
22 Mar 2024

Chem. Commun., 2024,60, 4455-4458

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

Z. Liao, F. Gao, Y. Ye, Q. Yu, C. Yang, Q. Luo, F. Du, B. Pan, W. Zhong and W. Liang, Chem. Commun., 2024, 60, 4455 DOI: 10.1039/D4CC00690A

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