Reactions of enamines with fluorinated acyl chlorides — Synthesis of fluorinated 1,3-diketones and 1,3-keto-aldehydes
✍ Scribed by He Hai-Ying; Qu Yan-Ling; Zhao Cheng-Xue
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 485 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0256-7660
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✦ Synopsis
The reactiom of enamina (la-b, 4, 6 ) with fluorinated acyl chlorida (2.4) produced fluorinated 1,3-diketona (3a-O and 1,3-keto-aldehyda (7a-c) in good yieldr M well M byproductr fluorinated acykmida ((k-c). It ir pro& that the resctionm involve nuckophilic attack by the Catom and/or N-atom of the enamina on scyl carbon of the fluorinated acyl chlorida.
📜 SIMILAR VOLUMES
## Abstract The N‐heterocyclic carbene‐catalyzed reaction of alkynyl aldehydes with 1,3‐keto esters or 1,3‐diketones has been studied. This protocol offers an entirely new, mild and atom‐economical access to highly functionalized 3,4‐dihydropyranones.
## Abstract The optimized method can be performed atom‐economically under mild conditions to afford highly functionalized 3,4‐dihydropyranones.
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