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◆ Chemical communications (Cambridge, England)2026-08-25

Convenient access to alkenylated indolo[2,1-a]isoquinolines via palladium-catalyzed cascade Heck cyclization/carbene insertion.

Xingyu Yuan, Yamin Dong, Yuhang Wang, Hongbo Qi, Shufeng Chen

原始摘要(英文原文)· Original abstract
A palladium-catalyzed cascade reaction of N-acryloyl indoles with hydrazones has been developed for the synthesis of alkenylated indolo[2,1-a]isoquinolines. This transformation proceeds through an intramolecular Heck cyclization followed by carbene capture, migratory insertion, and β-hydride elimination. Broad substrate compatibility was demonstrated for both hydrazones and N-acryloyl indoles, affording the desired products in moderate to excellent yields.
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Convenient access to alkenylated indolo[2,1-a]isoquinolines via palladium-catalyzed cascade Heck cyclization/carbene insertion. — 科研速览 Science Skim