## Abstract For Abstract see ChemInform Abstract in Full Text.
Efficient Synthesis of 14C-Labeled 1H-Pyrazolo[3,4-d]pyrimidine and Related [4.3.0]-Bicyclic Pyrimidino Systems
✍ Scribed by Jonathan Z. Ho; Kyle R. Van Arsdale; Matthew P. Braun
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- German
- Weight
- 174 KB
- Volume
- 91
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
In support of a research program aimed at discovering purine‐related anticancer drug candidates, a method for the ^14^C‐labeling of pyrazolopyrimidines utilizing the readily available labeled starting material, sodium [^14^C]formate, has been developed with a good overall yield. This new method was proven to be general in the preparation of other related [4.3.0]heterocycles containing N, O, and S atoms. A concise synthesis of a model compound, 8‐aza‐7‐deaza‐5′‐[^14^C]noraristeromycin, was achieved utilizing this methodology as a key step.
📜 SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract A series of new 1__H__‐pyrazolo[3,4‐__d__]pyrimidin‐4(__5H__)‐one Derivatives **5** has been designed and regio‐selectively synthesized __via__ a tandem aza‐Wittig reaction. The structures of all compounds prepared have been confirmed by ^1^H NMR, IR, EI‐MS spectroscopy and elemental an
## Abstract Allopurinol and 4‐amino‐1H‐pyrazolo[3,4‐d]pyrimidine N^1^‐and N^2^‐(D‐arabinofuranosides) have been synthesized. Nucleobase anion glycosylation of 4‐methoxy‐1H‐pyrazolo[3,4‐d]‐pyrimidine (7) with the α‐D‐arabinofuranosyl chloride 6a proceeds stereoselectively and affords the N^1^‐(β‐D‐n
## Abstract For Abstract see ChemInform Abstract in Full Text.