Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/18155
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dc.contributor.authorRubina, M. Y.-
dc.contributor.authorРубина, М. Ю.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2021-09-13T08:38:00Z-
dc.date.available2021-09-13T08:38:00Z-
dc.date.issued2021-
dc.identifier.citationYamanushkin, P. M.; Rubina, M. Y.; Rubin, M. A. Amide-directed reactions of small carbocycles // CURRENT ORGANIC CHEMISTRY. - 2021. - Volume 25. - Issue 14. - Page 1686-1703ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/18155-
dc.description.abstractThe topic of this review is the amide-directed functionalization of strained carbocycles - specifically, unsaturated or saturated three- and four-membered rings. The following approaches are discussed: a) directed carbometallation and hydrometallation of cyclopropenes catalyzed by transition metals; b) directed metal-templated nucleophilic addition reactions; c) directed C-H functionalization, including transition metal-catalyzed C-H-activation reactions; and d) directed radical additionsru
dc.language.isoenru
dc.publisherBENTHAM SCIENCE PUBL LTDru
dc.relation.ispartofseriesCurrent Organic Chemistry-
dc.subjectSmall cyclesru
dc.subjectDirecting groupsru
dc.subjectNucleophilic additionru
dc.subjectC-H activationru
dc.subjectC-H activationru
dc.subjectRadical additionsru
dc.titleAmide-directed reactions of small carbocyclesru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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