Reissert compound studies. XXI. Arylation reactions
The anions derived from both the isoquinoline and the quinoline Reissert compounds have been arylated by use of nitro and dinitro arylhalides. p-Fluorobenzaldehyde reacts preferentially at the carbonyl group and does not lead to arylation.
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| Veröffentlicht in: | Canadian journal of chemistry 1969-09, Vol.47 (17), p.3261-3263 |
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| Hauptverfasser: | , |
| Format: | Artikel |
| Sprache: | eng |
| Online-Zugang: | Volltext |
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| Zusammenfassung: | The anions derived from both the isoquinoline and the quinoline Reissert compounds have been arylated by use of nitro and dinitro arylhalides. p-Fluorobenzaldehyde reacts preferentially at the carbonyl group and does not lead to arylation. |
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| ISSN: | 0008-4042 1480-3291 |
| DOI: | 10.1139/v69-538 |