A convenient synthesis of 8-azaadenosine
β Scribed by John A. Montgomery; H. Jeanette Thomas; Sarah J. Clayton
- Book ID
- 112122094
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1970
- Tongue
- English
- Weight
- 192 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The annulation of isoquinoline derivatives to form the 8-oxoprotostep of the reaction involves intra-berbefine molecular derivatives is described. The key alkylation of the Reissert compounds.
The synthesis of 8-azaadenosine (la; z8A) has been performed by SnCI,-catalyzed glycosylation of X-azaadeninc (4) with I ,2,3.5-tetra-O-acetyl-/7-~-rihofuranose (5). followed by the separation of the regioisomers 6 and 7 and subsequent deacetylation. The ribonucleoside la as well as its 2.'-deoxy de
## Abstract For Abstract see ChemInform Abstract in Full Text.