A novel convenient one step pyrimidine synthesis
โ Scribed by A.L. Weis; V. Rosenbach
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 118 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
A new method for the preparation of pyrimidines by condensation of B-dicarbonyl compounds, ammonium salts and carbonyl containing substances has been developed.
An attractive approach to the synthesis of 1,2_dihydropyrimidines bearing alkyl or aryl groups consists of the reaction of B-dicarbonyl compounds, ammonium salts and carbonyl containing substances. 1,2_Dihydropyrimidines containing gem-dialkyl groups attached to the saturated carbon in position 2 of the pyrimidine ring have been prepared. l-3 These compounds are stable to further oxidation to pyrimidines because of the gem-disubstitution. New routes
๐ SIMILAR VOLUMES
A Convenient One-Step Gingerol Synthesis. -A facile one-step synthesis of racemic gingerol derivatives (III) by addition of aldehydes to the dianion of zingerone (I) is reported. The corresponding shogaols (IV) can be obtained by acid treatment of the corresponding gingerols. -(FLEMING,