Visible Light-Induced Intermolecular Dearomatization for Constructing Angularly Fused Tetracyclic Scaffolds

Visible light-induced dearomative cycloaddition has emerged as a powerful strategy for constructing complex polycyclic frameworks from simple aromatic precursors. Angularly fused polycyclic systems, which exhibit distinctive structural rigidity and tunable physicochemical properties, represent privileged scaffolds in bioactive natural products and pharmaceuticals. Herein, we report a robust photocatalytic protocol for the direct assembly of angularly fused tetracyclic scaffolds through intermolecular dearomatization of benzothiophene/indole derivatives with N-aryl cyclopropylamines. This transformation is achieved via a mechanistically intriguing cascade involving photocatalytic dearomative [3 + 2] cycloaddition and subsequent cyclization. This work demonstrates the synthetic feasibility of photocatalytic intermolecular dearomative [3 + 2] processes, providing direct access to structurally distinct angularly fused tetracyclic cores. Visible light-driven dearomative cycloadditions have become a powerful tool for building complex polycyclic frameworks from simple aromatics. Here, the authors report a photocatalytic strategy to assemble angularly fused tetracycles via intermolecular [3 + 2] dearomatization cascades.

Authors

Institutions

Publication Details

Journal
Nature Communications
Published
2026-06-30
DOI
https://doi.org/10.1038/s41467-026-75078-6
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Visible Light-Induced Intermolecular Dearomatization for Constructing Angularly Fused Tetracyclic Scaffolds

Tingting Song, Qing‐An Chen, Boshun Wan, Fan Lin et al.
Nature Communications
Radical Photochemical Reactions
article

Visible Light-Induced Intermolecular Dearomatization for Constructing Angularly Fused Tetracyclic Scaffolds

Tingting Song, Qing‐An Chen, Boshun Wan, Fan Lin, Ye Lu, Ya‐Guang Sun, Li Zhang, Zhi-Yuan Ding, Yilitabaier Julaiti
article en

Abstract

Visible light-induced dearomative cycloaddition has emerged as a powerful strategy for constructing complex polycyclic frameworks from simple aromatic precursors. Angularly fused polycyclic systems, which exhibit distinctive structural rigidity and tunable physicochemical properties, represent privileged scaffolds in bioactive natural products and pharmaceuticals. Herein, we report a robust photocatalytic protocol for the direct assembly of angularly fused tetracyclic scaffolds through intermolecular dearomatization of benzothiophene/indole derivatives with N-aryl cyclopropylamines. This transformation is achieved via a mechanistically intriguing cascade involving photocatalytic dearomative [3 + 2] cycloaddition and subsequent cyclization. This work demonstrates the synthetic feasibility of photocatalytic intermolecular dearomative [3 + 2] processes, providing direct access to structurally distinct angularly fused tetracyclic cores. Visible light-driven dearomative cycloadditions have become a powerful tool for building complex polycyclic frameworks from simple aromatics. Here, the authors report a photocatalytic strategy to assemble angularly fused tetracycles via intermolecular [3 + 2] dearomatization cascades.

Nature Communications
Shenyang University of Technology (CN), Dalian Institute of Chemical Physics (CN), Chinese Academy of Sciences (CN), University of Chinese Academy of Sciences (CN), Shenyang University of Chemical Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 14%
Radical Photochemical Reactions
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.