Synthesis of 3-(6-alkylaminopurin-9-yl)-2,3-dideoxy-D-thero-pentopyranoses and their reduction to 3-(6-alkylaminopurin-9-yl)-2,3-dideoxy-D-thero-pentitols
โ Scribed by Hans Peter Hjuler-Nielsen; Hans Pedersen; Henning Bue Hansen; Erik B. Pedersen; Claus Nielsen
- Book ID
- 112130311
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1992
- Tongue
- English
- Weight
- 182 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0022-152X
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๐ SIMILAR VOLUMES
A novel synthesis of AzddMAP and AzddGuo is described starting from 1, ## 2-0-isopropylidene-alpha-D-xylofuranose. The key step in this synthesis involves the replacement of a diphenyl carbamoyl protecting group in the purine 6-position by methanol. In 1987 Hartmann, Hunsmann, and Eckstein (1) re
## 3- [ N"-(4-C hlorp henyt)-l-met hyl-9-adenyl]-2.3-dideoxy-~-lbreopcntopyranosc (1) has been converted into the alkyl 3-[P-(4clila rop henyl)-2-me thyI-9-adenyl]-2,3-dideoxy-o-rhreo-pento~yraiiosides 2 and into thc N-aryl-3-~N6~4-chlorophenyl)-2-methyl-~)-adc:nyl]-2.3-dideoxy-~-fhreo-pcntopyrano