废止
催化作用
化学
烷基化
戒指(化学)
苯并呋喃
组合化学
三唑
氧化还原
立体化学
有机化学
作者
Silvia Cattani,Neeraj Kumar Pandit,Michele Buccio,Davide Balestri,Lutz Ackermann,Gianpiero Cera
标识
DOI:10.1002/anie.202404319
摘要
We report an unprecedented iron‐catalyzed C−H annulation using readily available 2‐vinylbenzofurans as the reaction pattern. The redox‐neutral strategy, based on cheap, non‐toxic and earth abundant iron catalysts, exploits triazole assistance to promote a cascade C−H alkylation, benzofuran ring‐opening and insertion into a Fe−N bond, to form highly functionalized isoquinolones. Detailed mechanistic studies supported by DFT calculations fully disclosed the manifold of the iron catalysis.
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