Please use this identifier to cite or link to this item:
https://dspace.ncfu.ru/handle/20.500.12258/2765| Title: | Directed nucleophilic addition of phenoxides to cyclopropenes |
| Authors: | Aksenov, N. A. Аксенов, Н. А. Rubin, M. A. Рубин, М. А. |
| Keywords: | Alkali metals;Carboxamides;Cyclopropene;Double bond;Nucleophilic addition;Templated;Addition reaction |
| Issue Date: | 2017 |
| Publisher: | Royal Society of Chemistry |
| Citation: | Yamanushkin, P., Lu-Diaz, M., Edwards, A., Aksenov, N.A., Rubina, M., Rubin, M. Directed nucleophilic addition of phenoxides to cyclopropenes // Organic and Biomolecular Chemistry. - 2017. - Volume 15. - Issue 38. - Pages 8153-8165 |
| Series/Report no.: | Organic and Biomolecular Chemistry |
| Abstract: | The alkali metal-templated addition of aryloxides across the double bond of non-conjugated cyclopropenes is described. High cis-selectivity is achieved through a directing effect of a strategically positioned carboxamide functionality |
| URI: | http://hdl.handle.net/20.500.12258/2765 |
| Appears in Collections: | Статьи, проиндексированные в SCOPUS, WOS |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| scopusresults 205 .pdf Restricted Access | 62.48 kB | Adobe PDF | View/Open | |
| WoS 96 .pdf Restricted Access | 45.21 kB | Adobe PDF | View/Open |
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