Synthesis of 4-Substituted 1-((2,3-Dihydroxy-1-propoxy)methyl)-1Hpyrazolo (3,4-d)pyrimidines. -The regioselective synthesis of a series of acyclonucleosides of pyrazolopyrimidines (cf. (IV), (V), (VII), (IX)) is described. The obtained compounds are evaluated for their cytotoxicity and anti-HIV act
ChemInform Abstract: Several Approaches to Cyanide Ion-Catalyzed Synthesis of 4-Aroyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidines.
β Scribed by A. MIYASHITA; Y. SUZUKI; K. OHTA; K. IWAMOTO; T. HIGASHINO
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 29 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Several Approaches to Cyanide Ion-Catalyzed Synthesis of 4-Aroyl-1-phenyl-1H-pyrazolo [3,4-d]pyrimidines.
-The reaction of the 4-chloropyrimidine (I) with aromatic aldehydes (II) gives the 4-aroyl derivatives (III) in the presence of catalytic p-toluenesulfinate and potassium cyanide. The yields are substantially higher compared to the reactions using catalytic KCN only. Furthermore, the analogous 4-tosylpyrimidine (IV) provides good yields using KCN as sole catalyst, showing the tosyl group to be a more effective leaving group. -(MIYASHITA, A.;
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v