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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/2974
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dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorAksenova, I. V.-
dc.contributor.authorАксенова, И. В.-
dc.date.accessioned2018-09-14T08:43:35Z-
dc.date.available2018-09-14T08:43:35Z-
dc.date.issued2017-
dc.identifier.citationLevashov, A.S., Aksenov, N.A., Aksenova, I.V., Konshin, V.V. Oxidative coupling of tetraalkynyltin with aldehydes leading to alkynyl ketones // New Journal of Chemistry. - 2017. - Volume 41. - Issue 16. - Pages 8297-8304ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/2974-
dc.description.abstractThe reaction of tetraalkynyltin with aldehydes was studied for the first time. The reaction was shown to proceed as a tandem process of nucleophilic addition of tin acetylide to aldehyde followed by Oppenauer-type oxidation of produced tin alcoholates, and may be used as a convenient one-pot approach to acetylenic ketones. The advantages and limitations of the proposed method are discussedru
dc.language.isoenru
dc.publisherRoyal Society of Chemistryru
dc.relation.ispartofseriesNew Journal of Chemistry-
dc.subjectAldehyde derivativeru
dc.subjectKetone derivativeru
dc.subjectStannic chlorideru
dc.subjectOxidative couplingru
dc.titleOxidative coupling of tetraalkynyltin with aldehydes leading to alkynyl ketonesru
dc.typeСтатьяru
vkr.amountPages 8297-8304ru
vkr.instИнститут математики и естественных наук-
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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