4.8 Article

Synthesis of Ester-Substituted Indolo[2,1-a]isoquinolines via Photocatalyzed Alkoxycarbonylation/Cyclization Reactions

Journal

ORGANIC LETTERS
Volume 24, Issue 2, Pages 642-647

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.1c04082

Keywords

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Funding

  1. National Natural Science Foundation of China [21871053]
  2. Leading Innovative and Entrepreneur Team Introduction Program of Zhejiang [2019R01005]
  3. Open Research Fund of School of Chemistry and Chemical Engineering, Henan Normal University [2020ZD04]

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A direct alkoxycarbonylation/cyclization reaction is achieved through visible light-induced photoredox catalysis, leading to the synthesis of ester-substituted indolo[2,1-a]isoquinolines in good to excellent yields. This method offers an alternative route for the construction of complex target structures bearing carboxylic esters.
A direct alkoxycarbonylation/cyclization reaction is accomplished under visible light-induced photoredox catalysis. With this approach, a variety of ester-substituted indolo[2,1-a]isoquinolines are prepared in good to excellent yields. It is worth noting that this method not only can afford the synthesis of indolo[2,1-a]isoquinolines but also can provide an alternative route for generating complex target structures bearing carboxylic esters.

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