Synthesis of Benzofuran Derivatives through Cascade Radical Cyclization/Intermolecular Coupling of 2‐Azaallyls

Benzofurans are among the most popular structural units in bioactive natural products, however, the synthesis of such structures by radical cyclization cascade reactions is rare. Herein, we report a mild and broadly applicable method for the construction of complex benzofurylethylamine derivatives t...

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Veröffentlicht in:Angewandte Chemie International Edition 2019-02, Vol.58 (9), p.2826-2830
Hauptverfasser: Deng, Guogang, Li, Minyan, Yu, Kaili, Liu, Chunxiang, Liu, Zhengfen, Duan, Shengzu, Chen, Wen, Yang, Xiaodong, Zhang, Hongbin, Walsh, Patrick J.
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Sprache:eng
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Zusammenfassung:Benzofurans are among the most popular structural units in bioactive natural products, however, the synthesis of such structures by radical cyclization cascade reactions is rare. Herein, we report a mild and broadly applicable method for the construction of complex benzofurylethylamine derivatives through a unique radical cyclization cascade mechanism. Single‐electron transfer (SET) from 2‐azaallyl anions to 2‐iodo aryl allenyl ethers initiates a radical cyclization that is followed by intermolecular radical–radical coupling. This expedient approach enables the synthesis of a range of polycyclic benzofurans that would otherwise be difficult to prepare. Well behaved radicals: a mild and broadly applicable method for the construction of complex benzofurylethylamine derivatives through a unique radical cyclization cascade mechanism is presented. SET from 2‐azaallyl anions to 2‐iodo aryl allenyl ethers initiates a radical cyclization that is followed by intermolecular radical–radical coupling.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201812369