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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/2765
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dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2018-08-03T12:47:55Z-
dc.date.available2018-08-03T12:47:55Z-
dc.date.issued2017-
dc.identifier.citationYamanushkin, 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 8153-8165ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/2765-
dc.description.abstractThe 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 functionalityru
dc.language.isoenru
dc.publisherRoyal Society of Chemistryru
dc.relation.ispartofseriesOrganic and Biomolecular Chemistry-
dc.subjectAlkali metalsru
dc.subjectCarboxamidesru
dc.subjectCyclopropeneru
dc.subjectDouble bondru
dc.subjectNucleophilic additionru
dc.subjectTemplatedru
dc.subjectAddition reactionru
dc.titleDirected nucleophilic addition of phenoxides to cyclopropenesru
dc.typeСтатьяru
vkr.amountPages 8153-8165ru
vkr.instИнститут математики и естественных наук-
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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