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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/395
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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.accessioned2018-05-31T14:52:57Z-
dc.date.available2018-05-31T14:52:57Z-
dc.date.issued2018-
dc.identifier.citationMaslivetc, V., Barrett, C., Aksenov, N.A., Rubina, M., Rubin, M. Intramolecular nucleophilic addition of carbanions generated from: N -benzylamides to cyclopropenes // Organic and Biomolecular Chemistry. - 2018. - Volume 16. - Issue 2. - pp. 285-294.ru
dc.identifier.urihttps://dspace.ncfu.ru:443/handle/20.500.12258/395-
dc.description.abstractAn unusual reaction is described, involving a formal intramolecular nucleophilic substitution of bromocyclopropanes with nitrogen ylides generated in situ from N-benzyl carboxamides. It is shown that this reaction involves cyclopropene intermediates and allows for the facile and expeditious preparation of 3-azabicyclo[3.1.0]hexan-2-one scaffoldsru
dc.language.isoenru
dc.publisherRoyal Society of Chemistryru
dc.relation.ispartofseriesOrganic and Biomolecular Chemistry-
dc.subjectAddition reactionru
dc.subjectScaffoldsru
dc.subjectCarboxamidesru
dc.subjectCyclopropeneru
dc.subjectNucleophilic additionru
dc.subjectNucleophilic substitutionsru
dc.subjectReaction intermediateru
dc.titleIntramolecular nucleophilic addition of carbanions generated from: N -benzylamides to cyclopropenesru
dc.typeСтатьяru
vkr.amountPages 285-294ru
vkr.instИнститут математики и естественных наук-
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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