Azines and Azoles: CXXII. New Regioselective Synthesis of 1-Substituted 6-Alkyluracils
β Scribed by V. N. Yuskovets; A. V. Moskvin; L. E. Mikhailov; B. A. Ivin
- Publisher
- Springer
- Year
- 2005
- Tongue
- English
- Weight
- 114 KB
- Volume
- 75
- Category
- Article
- ISSN
- 1070-3632
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Many naturally occurrinq as well as synthetic nucleosides are known to manifest a variety of bioloqical activities (l-3) . Very often these compounds are pyrimidine type analoques of the normal nucleic acid constituents in which the C-5, C-6 double bond has been functionalized. Thus several C-S subs
## Abstract For Abstract see ChemInform Abstract in Full Text.
A simple synthesis of 5-acyl-4-hydroxy-3,6-dihydro-2H-1,3-thiazine-2,6-diones from malonic acid, potassium thiocyanate and acid anhydrides is described. A new, general, regioselective method for the synthesis of 1-substituted-6-alkyluracils by the reaction of these thiazines with primary alkyl and a
A number of substituted 2,2-dimethyl-6-arylidene-1-triazol-1ylmethylcyclohexanols and 2,2-dimethyl-6-arylidene-1-imidazol-1-ylmethylcyclohexanols were prepared from 2-methylcyclohexanone in four steps : ClaisenΓ Schmidt condensation with substituted benzaldehydes, methylation of the resulting 2-meth
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.