- Combes Quinoline Synthesis
-
Combes Synthesis
A. Combes, Bull. Soc. Chim. France 49, 89 (1888).
Formation of quinolines by condensation of β-diketones with primary arylamines followed by acid-catalyzed ring closure of the intermediate Schiff base:

W. S. Johnson, F. J. Matthews, J. Am. Chem. Soc. 66, 210 (1944); F. W. Bergstrom, Chem. Rev. 35, 156 (1944); J. C. Perche et al., J. Chem. Soc. Perkin Trans. I 1972, 260; J. Born, J. Org. Chem. 37, 3952 (1972). Cf. Conrad-Limpach Reaction; Doebner Reaction.
Prev: Conrad-Limpach Cyclization
Next: Gabriel-Colman Rearrangement - 【Back】【Close 】【Print】【Add to favorite 】
- Related information
- International Priceso of Synthesis Ammonia in the Falling Trends
- International Prices of Synthesis Ammonia in Falling Trends
- International Prices of Synthesis Ammonia in Falling Trends
- International Prices of Synthesis Ammonia in Differentiation Trends
- International Prices of Synthesis Ammonia in Differentiation Trends
- International Prices of Synthesis Ammonia in Rising Trend
- International Prices of Synthesis Ammonia in Rising Trend
- International Prices of Synthesis Ammonia in Rising Trend
- International Prices of Synthesis Ammonia in Rising Trend
- International Prices of Synthesis Ammonia in Early September
-
Health and Chemical more >
-
Hot Products
- 844683-39-2 4-Chloro-3',4'-dimethoxybenzhydrol
- 9003-97-8 Polycarbophil
- 72244-98-5 Polyoxy(methyl-1,2-ethanediyl), .alpha.-hydro-.omega.-hydroxy-, ether with 2,2-bis(hydroxymethyl)-1,3-propanediol (4:1), 2-hydroxy-3-mercaptopropyl ether
- 28497-59-8 GLYCEROL 1,3-DIMETHACRYLATE
- 343373-23-9 2-chloro-N-(5-iodo-2-pyridinyl)acetamide
- 10294-34-5 Borane, trichloro-
- 486460-32-6 Sitagliptin
- 66-84-2 D-Glucosamine hydrochloride
- 126208-12-6 SNARF-1
- 14548-72-2 1,1'-(cyclohexylimino)bispropan-2-ol
- 915095-99-7 (1S)-1,5-anhydro-2,3,4,6-tetra-O-acteyl-1-C-[4-chloro-3-[[4-[[(3S)-tetrahydrofu-ran-3-yl]oxy]phenyl] methyl]phenyl]-D-Glucitol
- 312739-92-7 TRIS(BUTYLCYCLOPENTADIENYL)SCANDIUM(III&


