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Synthesis of benzo[f]quinoline derivatives by condensation of N-arylmethylene-2-naphthylamines with acetylcyclohexane and 1-acetylcyclohexene
| Content Provider | Semantic Scholar |
|---|---|
| Author | Grachek, V. I. |
| Copyright Year | 2004 |
| Abstract | N-Arylmethylene-2-naphthylamines react with acetylcyclohexane and 1-acetylcyclohexene under mild conditions to afford 2-aryl-2-(2-naphthylamino)ethyl cyclohexyl and 1-cyclohexenyl ketones, respectively. Under more severe conditions (110°C), the reaction is accompanied by cyclization with formation of 3-aryl-1-cyclohexyl(or 1-cyclohexenyl)benzo[f]quinolines. Proper choice of the amount of catalyst, temperature, and reaction time allows isolation of intermediate 3-aryl-1-cyclohexyl(or 1-cyclohexenyl)-3,4-dihydrobenzo[f]quinolines. |
| Starting Page | 1748 |
| Ending Page | 1753 |
| Page Count | 6 |
| File Format | PDF HTM / HTML |
| DOI | 10.1007/s11176-005-0094-4 |
| Volume Number | 74 |
| Alternate Webpage(s) | https://page-one.springer.com/pdf/preview/10.1007/s11176-005-0094-4 |
| Alternate Webpage(s) | https://doi.org/10.1007/s11176-005-0094-4 |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |