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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.urihttps://www.scopus.com/record/display.uri?eid=2-s2.0-85027030617&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=1af4e03e943ebe5b20c0bfa6c2ca02b9&sot=afnl&sdt=sisr&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&ref=%28Oxidative+coupling+of+tetraalkynyltin+with+aldehydes+leading+to+alkynyl+ketones%29&relpos=1&citeCnt=3&searchTerm=-
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-
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