Carbocyclic analogs of 5'-amino-5'deoxy- and 3'-amino-3'-deoxythymidines
✍ Scribed by Shealy, Y. Fulmer; O'Dell, C. Allen; Shannon, William M.; Arnett, Gussie
- Book ID
- 126333206
- Publisher
- American Chemical Society
- Year
- 1986
- Tongue
- English
- Weight
- 731 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0022-2623
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📜 SIMILAR VOLUMES
3'-Amino-3'-deoxythymidine was converted, in multi-steps, to its 5'-O-(4,4'-dimethoxytrityl)-5'-C-tosyloxyethyl-3'-N-carbobenzoxy derivative 7 and 5'-C-mesyloxyethyl-3'-N-(9-fluorenyl)methoxycarbonyl derivatives 6 and 11. Subsequent hydrogenolysis or treatment with DMAP afforded 3'-N,5'-C-bridged bi
The syntheses have been described of the 2-acetamido-2-deoxy derivatives of 5-thio-D-glucose lm3, 5-thio-D-mannose 4, 5-thio-D-allose 5, 3-acetamido-3-deoxy5thio-D-xylose6, and 4-acetamido-4-deoxy-5-thio-r\_-lyxose6. We now report the syntheses of 3-amino-3-deoxy-5-thio-D-allose hydrochloride and a
## Abstract A synthesis of 3′‐amino‐3′, 5′‐dideoxyadenosine is described. This compound is not a substrate of adenosine deaminase.