Studies on Tertiary Amine Oxides. LIII. Studies on Preparation and Properties of 3, 2'-Diquinolyl N-Oxides
N-Oxidation of 3, 2'-diquinolyl (4) was examined under various conditions to give the 1-oxide (5) and 1, 1'-dioxide (6). The 1-oxide group in 5 and 6 was easily deoxygenated by heating with carbon disulfide in N, N-dimethylformamide (DMF); the 1'-oxide group resisted this deoxygenatio...
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Veröffentlicht in: | YAKUGAKU ZASSHI 1975/09/25, Vol.95(9), pp.1078-1084 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | jpn |
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Online-Zugang: | Volltext |
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Zusammenfassung: | N-Oxidation of 3, 2'-diquinolyl (4) was examined under various conditions to give the 1-oxide (5) and 1, 1'-dioxide (6). The 1-oxide group in 5 and 6 was easily deoxygenated by heating with carbon disulfide in N, N-dimethylformamide (DMF); the 1'-oxide group resisted this deoxygenation. This indicates that 1-oxide function has a slight nitrone-like property, and this was supported by the fact that nitation of 5 did not give γ- or α-nitro compound. |
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ISSN: | 0031-6903 1347-5231 |
DOI: | 10.1248/yakushi1947.95.9_1078 |