Synthesis of 2-azido-1-methyl-aminobenzimidazole
β Scribed by O. V. Dyablo; A. F. Pozharskii
- Publisher
- Springer US
- Year
- 1999
- Tongue
- English
- Weight
- 186 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0009-3122
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## Abstract A novel class of 5β(1βazidoβ2βhaloethyl)arabinouridines 4β6 was synthesized by the regiospecific addition of halogenoazides (XN~3~: X = C1, Br, I) to the vinyl substituent of 5βvinylarabinouridine (7). The title 5β(1βazidoβ2βhaloethyl)arabinouridines 4β6 were previously shown to exhibit
Axidoquinones (1) have been shown to undergo a variety of interesting transformations. a ' ' -butenolides, 1 2 3 Y -Cyanoalkylidine-y 2-cyano-1,3-cyclopentenediones, cyanoketenes, axapinediones, 4 and acylcyanides5 can be prepared from azidoquinones (1) by employing the appro-