Synthesis of 5-substituted uracils and 2,4-dimethoxypyrimidines by wittig olefination
A variety of new 5‐alkenyluracils has been prepared in high yields by Wittig olefination of 5‐formyl‐1‐octy‐luracil, 5‐formyl‐1,3‐dioctyluracil and 5‐formyl‐2,4‐dimethoxy pyrimidine with stabilized and semistabi‐lized phosphorus ylides. The conformation of the products is discussed on the basis of 1...
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Veröffentlicht in: | Journal of heterocyclic chemistry 2005-09, Vol.42 (6), p.1135-1142 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | A variety of new 5‐alkenyluracils has been prepared in high yields by Wittig olefination of 5‐formyl‐1‐octy‐luracil, 5‐formyl‐1,3‐dioctyluracil and 5‐formyl‐2,4‐dimethoxy pyrimidine with stabilized and semistabi‐lized phosphorus ylides. The conformation of the products is discussed on the basis of 1H NMR spectral data. |
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ISSN: | 0022-152X 1943-5193 |
DOI: | 10.1002/jhet.5570420615 |