A novel ring transformation of 5-azidothiazoles
β Scribed by Erik Ceulemans; Leonard K. Dyall; Wim Dehaen
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 516 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
The 4-oxoalkyl-and 4-iminoaikyl-5-azidothiazoles undergo a ring transformation with nitrogen loss at relatively low temperatures to afford 4-cyanooxazoles and 4-cyanoimidazoles, respectively. The mechamsm, wMch ts thought to revolve a ring openmg-rmg closure process, is discussed.
π SIMILAR VOLUMES
Treatment of 1,3-disubstituted 5-nitrouracils(5) with malonamide in ethanolic sodium ethoxide caused a ring transformation to afford l-substituted 5-carbamoyluracils(6) in good yields. Reactions of uracil derivatives with various nucleophiles have been extensively investigated in connection with bio