Directed nucleophilic addition of phenoxides to cyclopropenes
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
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Royal Society of Chemistry
2018
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oai:10.200.131.19:20.500.12258-27652018-09-05T14:07:33Z Directed nucleophilic addition of phenoxides to cyclopropenes Aksenov, N. A. Аксенов, Н. А. Rubin, M. A. Рубин, М. А. Alkali metals Carboxamides Cyclopropenes Double bonds Nucleophilic additions Templated Addition reactions 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 2018-08-03T12:47:55Z 2018-08-03T12:47:55Z 2017 Статья 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 https://www.scopus.com/record/display.uri?eid=2-s2.0-85030682886&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=North+Caucasus+Federal+University&sid=a75f219f53d4022b97f1d2161feb9566&sot=afnl&sdt=sisr&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&ref=%28Directed+nucleophilic+addition+of+phenoxides+to+cyclopropenes%29&relpos=2&citeCnt=2&searchTerm= http://hdl.handle.net/20.500.12258/2765 en Organic and Biomolecular Chemistry application/pdf application/pdf Royal Society of Chemistry |
| institution |
СКФУ |
| collection |
Репозиторий |
| language |
English |
| topic |
Alkali metals Carboxamides Cyclopropenes Double bonds Nucleophilic additions Templated Addition reactions |
| spellingShingle |
Alkali metals Carboxamides Cyclopropenes Double bonds Nucleophilic additions Templated Addition reactions Aksenov, N. A. Аксенов, Н. А. Rubin, M. A. Рубин, М. А. Directed nucleophilic addition of phenoxides to cyclopropenes |
| description |
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 |
| format |
Статья |
| author |
Aksenov, N. A. Аксенов, Н. А. Rubin, M. A. Рубин, М. А. |
| author_facet |
Aksenov, N. A. Аксенов, Н. А. Rubin, M. A. Рубин, М. А. |
| author_sort |
Aksenov, N. A. |
| title |
Directed nucleophilic addition of phenoxides to cyclopropenes |
| title_short |
Directed nucleophilic addition of phenoxides to cyclopropenes |
| title_full |
Directed nucleophilic addition of phenoxides to cyclopropenes |
| title_fullStr |
Directed nucleophilic addition of phenoxides to cyclopropenes |
| title_full_unstemmed |
Directed nucleophilic addition of phenoxides to cyclopropenes |
| title_sort |
directed nucleophilic addition of phenoxides to cyclopropenes |
| publisher |
Royal Society of Chemistry |
| publishDate |
2018 |
| url |
https://www.scopus.com/record/display.uri?eid=2-s2.0-85030682886&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=North+Caucasus+Federal+University&sid=a75f219f53d4022b97f1d2161feb9566&sot=afnl&sdt=sisr&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&ref=%28Directed+nucleophilic+addition+of+phenoxides+to+cyclopropenes%29&relpos=2&citeCnt=2&searchTerm= https://dspace.ncfu.ru/handle/20.500.12258/2765 |
| work_keys_str_mv |
AT aksenovna directednucleophilicadditionofphenoxidestocyclopropenes AT aksenovna directednucleophilicadditionofphenoxidestocyclopropenes AT rubinma directednucleophilicadditionofphenoxidestocyclopropenes AT rubinma directednucleophilicadditionofphenoxidestocyclopropenes |
| _version_ |
1760531710968070144 |