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- W3156585802 endingPage "2229" @default.
- W3156585802 startingPage "2223" @default.
- W3156585802 abstract "Described herein is the Rh(III)- catalyzed [3+2] annulations and C2-alkenylations of indoles with 1,3-diynes, which deliver the synthetically important 3H-pyrrolo[1,2-a]indol-3-ones and highly functionalized tetrasubstituted olefin derivatives. Importantly, in this methodology, the additive controlled selective formation of desired scaffolds. This synthetic strategy exhibits high efficiency and broad functional group compatibility. Furthermore, this protocol has been successfully extended to the synthesis of bis-annulated and trisubstituted alkenes. The method is also smoothly applied for the synthesis of the core structure of protein kinase C inhibitor and melatonin analogues." @default.
- W3156585802 created "2021-04-26" @default.
- W3156585802 creator A5054168920 @default.
- W3156585802 creator A5063290574 @default.
- W3156585802 creator A5069775143 @default.
- W3156585802 creator A5079478168 @default.
- W3156585802 date "2021-04-21" @default.
- W3156585802 modified "2023-09-27" @default.
- W3156585802 title "Rh(III)‐Catalyzed [3+2] Annulation and C−H Alkenylation of Indoles with 1,3‐Diynes by C−H Activation" @default.
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