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Reactions of methylenecyclopropanes with a diethylzinc-bromoform system, and the utilization for synthesis of a novel cyclopropylidene-nucleoside
✍ Scribed by Changmei Cheng; Tetsuro Shimo; Kenichi Somekawa; Masaru Kawaminami
- Book ID
- 104258401
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 211 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
The reactions of substituted me~hylanecyclopropane with clethylzinc-bromoform gave bromcepimf2.2]pentane d=ivatives, bromoform-aditien compounds, an oxabicydo-compound and adjacent di~pound, and the last ixcduct was derived to a novel a, ~unmanated nucloside.
📜 SIMILAR VOLUMES
## a b s t r a c t The sulfoxide-magnesium exchange reaction of aryl 1-chlorocyclopropyl sulfoxides with i-PrMgCl in THF at low temperature gave magnesium cyclopropylidenes. Treatment of the magnesium cyclopropylidenes with lithium naphtholates or phenolates resulted in the formation of spiro[2.6]n
## Abstract The synthesis of a novel ring‐expanded nucleoside analogue, (Z)‐1‐((2‐Guanidinocarbamoyl‐cyclopropylidene)methyl)‐4,5,7,8‐tetrahydro‐6__H__‐6‐iminoimidazo[4,5‐__e__][1,3]diazepine‐4,8‐dione (**1**) has been reported. It was prepared starting from methyl imidazole‐4,5‐dicarboxylate by se