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3-Trifloxy-3-trifluoromethylpropeniminium Triflate: Reaction with Aromatic Amines – An Efficient Synthesis of 2-Trifluoromethylquinolines
✍ Scribed by Ivan L. Baraznenok; Valentine G. Nenajdenko; Elizabeth S. Balenkova
- Book ID
- 101279125
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 232 KB
- Volume
- 1999
- Category
- Article
- ISSN
- 1434-193X
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✦ Synopsis
The reaction of iminium triflates 2 and 7 with various
The reactions of 2 and 7 with diarylamines proceeds, suprisingly, to afford the corresponding 3-R f -substituted aromatic amines were investigated. The 2-R f -substituted quinolines 3 and 8 were prepared in excellent yields by the cinnamaldehydes 4 and 9. reaction of 2 and 7, respectively, with substituted anilines.
📜 SIMILAR VOLUMES
Benzopyrano[2,3-b]pyridines were efficiently prepared by condensation of 1,3-bis-silyl enol ethers with 3-cyanobenzopyrylium triflates and subsequent domino 'retro-Michael-lactonization-aldol' reactions.
3-(aryl/ alkylimino)methylchromones 3-Anilino-2-salicyloylacrylonitriles a b s t r a c t 3-Cyanochromones react with primary aromatic amines to give 2-amino-3-(aryliminomethyl)chromones as the sole products or as their mixtures with Z-and E-3-anilino-2-salicyloylacrylonitriles, depending on the reac
By using a domino reaction of aromatic amines with various cyclic hemiacetals catalyzed by indium chloride in water, tetrahydroquinoline derivatives were synthesized efficiently.