Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/12117
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dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2020-06-25T13:11:19Z-
dc.date.available2020-06-25T13:11:19Z-
dc.date.issued2020-
dc.identifier.citationYamanushkin, P., Smith, S.P., Petillo, P.A., Rubin, M. Cyclopropene-Templated Assembly of Medium Cycles via Ru-Catalyzed Ring-Closing Metathesis // Organic Letters. - 2020. - Volume 22. - Issue 9. - Pages 3542-3546ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/12117-
dc.description.abstractAn expeditious click-click cyclize strategy for the assembly of medium-sized heterocyclic rings is described. The sequence involves the reaction of cycloprop-2-ene carboxylic acids with unsaturated amines to furnish amides, which are further subjected to a Cu-catalyzed directed carbomagnesiation and a ring-closing olefin metathesis reaction. This methodology allows for the efficient preparation of lactams with ring sizes up to 10ru
dc.language.isoenru
dc.publisherAmerican Chemical Societyru
dc.relation.ispartofseriesOrganic Letters-
dc.subjectCycloaddition Reactionru
dc.subjectCyclopropenesru
dc.subjectVinylcarbeneru
dc.titleCyclopropene-templated assembly of medium cycles via ru-catalyzed ring-closing metathesisru
dc.typeСтатьяru
vkr.instИнститут математики и естественных наукru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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