Synthesis of 6-mercapto-9-β-d-ribofuranosyl-purine 5′-triphosphate, a sulfhydryl analog of ATP
✍ Scribed by Alexander J. Murphy; Joseph A. Duke; Linda Stowring
- Book ID
- 115700831
- Publisher
- Elsevier Science
- Year
- 1970
- Tongue
- English
- Weight
- 150 KB
- Volume
- 137
- Category
- Article
- ISSN
- 0003-9861
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The allylic alcohol in ribose-protected zeatin riboside 1, was oxidised to an aldehyde by barium manganate. Heating of the resulting aldehyde in chloroform allowed the cyclizatiin of the N%hain into a 3methylpyrrole ring. After deprotection of the ribose, the title compound was obtained and identifi
A series of 6-substituted purine nucleosides have been synthesized in mcderate yield by the nickel catalyzed cross coupling reaction between alkyl-and aryl-Griqnard reagents and 2',3',5'-tris-@-(t-butyldimethylsilyl)-9-~-~-ribofuranosy1-6-chloropurine. Adenosine analogues with alkyl and aryl group l