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Visible‐Light‐Induced Oxidation/[3+2] Cycloaddition/Oxidative Aromatization Sequence: A Photocatalytic Strategy To Construct Pyrrolo[2,1‐a]isoquinolines

Zou, You‐Quan, Lu, Liang‐Qiu, Fu, Liang, Chang, Ning‐Jie, Rong, Jian, Chen, Jia‐Rong, Xiao, Wen‐Jing·2011·Angewandte Chemie

Abstract

Sonnige Aussichten: Durch die im Titel beschriebene Sequenz werden 2-(3,4-Dihydroisochinolin-2(1H)-yl)essigsäureethylester mit einer Reihe elektronenarmer Alkene und Alkine effizient in Pyrrolo[2,1-a]isochinoline umgewandelt (siehe Schema; bpy=2,2′-Bipyridin, EWG = elektronenziehende Gruppe). Die Reaktion bietet eine neue Strategie zum direkten Aufbau der Kernstruktur natürlicher Lamellarin-Alkaloide. Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

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Metadata

Authors
Zou, Y., Lu, L., Fu, L., Chang, N., Rong, J., Chen, J., & Xiao, W.
Venue
Angewandte Chemie
Publisher
Wiley
Published
2011-06-22
Volume
123
Issue
31
Pages
7309-7313
ISSN
  • 0044-8249 (ISSN-L)
  • 1521-3757
OpenAlex
W4245809625
Cited by
362
References
0
FWCI
25.59
Type
journal article
Language
de
Open access
closed

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CoChat. (2026). Citation check: Visible‐Light‐Induced Oxidation/[3+2] Cycloaddition/Oxidative Aromatization Sequence: A Photocatalytic Strategy To Construct Pyrrolo[2,1‐a]isoquinolines. https://app.cochat.ai/papers/10.1002/ange.201102306
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Zou, Y., Lu, L., Fu, L., Chang, N., Rong, J., Chen, J., & Xiao, W. (2011). Visible‐Light‐Induced Oxidation/[3+2] Cycloaddition/Oxidative Aromatization Sequence: A Photocatalytic Strategy To Construct Pyrrolo[2,1‐a]isoquinolines. Angewandte Chemie. https://doi.org/10.1002/ange.201102306

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