## Abstract The synthesis of 8‐azaguanine __N__^9^‐, __N__^8^‐, and __N__^7^‐(2′‐deoxyribonucleosides) 1–3, related to 2′‐deoxyguanosine (4), is described. Glycosylation of the anion of 5‐amino‐7‐methoxy‐3__H__‐1,2,3‐triazolo[4,5‐__d__]pyrimidine (5) with 2‐deoxy‐3,5‐di‐__O__‐(4‐toluoyl)‐α‐D‐__eryt
Synthesis of 2′-Deoxyribofuranosides of 8-Aza-7-deazaguanine and Related Pyrazolo[3,4-d]pyrimidines
✍ Scribed by Frank Seela; Herbert Steker
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- German
- Weight
- 845 KB
- Volume
- 69
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract Phase‐transfer glycosylation of 4‐methoxy‐1__H__‐pyrazolo[3,4‐__d__]pyrimidine with the 2‐deoxyribofuranosyl chloride **9** formed the N(1)‐β‐nucleoside **10a** as main product (39%). As by‐products the α‐D‐anomer **11a** (7%) and the N(2)‐isomer **12a** (18%) were isolated. Assignment
## Abstract Pyrazolo‐[3,4‐__d__]pyrimidine‐4,6‐diones **5** and pyrazolo[4,3‐__d__]pyrimidine‐5,7‐diones **7** were synthesized by Curtius rearrangement of pyrazolic mono‐esters **2** and **3** followed by hetero‐cyclization __via__ the ureas derivatives **4** and **6** under alkaline conditions.
Oligonucleotides containing 7-substituted 8-aza-7-deazaguanines ( 6-amino-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-ones) were prepared by automated solid-phase synthesis. A series of 7-alkynylated 8aza-7-deaza-2'-deoxyguanosines (see 4a ± d) were synthesized with the 7-iodonucleoside 3c as starting