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A convenient synthesis of 8-azaadenosine

✍ 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

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πŸ“œ SIMILAR VOLUMES


Structure of 8-azaadenosine hydrochlorid
✍ Singh, P. ;Hodgson, D. J. πŸ“‚ Article πŸ“… 1989 πŸ› International Union of Crystallography 🌐 English βš– 479 KB
A convenient synthesis of 8-oxoprotoberb
✍ Somsak Ruchirawat; Werawat Lertwanawatana; Pongtip Thepchumrune πŸ“‚ Article πŸ“… 1980 πŸ› Elsevier Science 🌐 French βš– 233 KB

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.

8-Azaadenosine and Its 2β€²-Deoxyribonucle
✍ Frank Seela; Ingo MΓΌnster; Uwe LΓΌchner; Helmut Rosemeyer πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 German βš– 995 KB

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

Convenient Synthesis of 8-Amino-2β€²-deoxy
✍ Miriam Frieden; Anna Avino; Ramon Eritja πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons βš– 133 KB πŸ‘ 1 views

## Abstract For Abstract see ChemInform Abstract in Full Text.