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One-pot access to indazole fused-phenanthridinones via Rh(III)-catalyzed [4+2] annulation

An efficient synthesis of indazole fused phenanthridinones via Rh(III)-catalyzed inert C(sp2)-H activation/[4 ​+ ​2] annulation of 3-aryl-1H-indazoles with iodonium ylides has been developed, providing a strategy to access multi-conjugated π-system tetracyclic and pentacyclic aza-heterocyclics with...

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Detaylı Bibliyografya
Asıl Yazarlar: Shumin Li, Jinke Chang, Jian Shen, Xiuling Cui
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: KeAi Communications Co. Ltd. 2025-02-01
Seri Bilgileri:Green Synthesis and Catalysis
Konular:
Online Erişim:http://www.sciencedirect.com/science/article/pii/S2666554923000789
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