Visible-light-induced oxidative ring expansion of indoles with amidines

Literature Information

Publication Date 2019-04-02
DOI 10.1039/C9QO00379G
Impact Factor 5.281
Authors

Ling-Ling Zhang, Wen-Bin Cao, Xiao-Ping Xu, Shun-Jun Ji


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Abstract

An efficient and mild visible-light-enabled reaction involving the oxidative ring expansion of indoles with amidines in the aqueous phase at room temperature is developed. Benzo[1,3,5]triazocin-6(5H)-ones and quinazolinones were facilely obtained as the terminal products by using 2-substituted indoles and substituent-free indoles as substrates, respectively. This protocol features mild conditions, excellent functional group tolerance, and moderate to good yields.

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Organic Chemistry Frontiers

Organic Chemistry Frontiers
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Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

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