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dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2018-12-17T14:00:18Z-
dc.date.available2018-12-17T14:00:18Z-
dc.date.issued2015-
dc.identifier.citationEdwards, A., Bennin, T., Rubina, M., Rubin, M. Synthesis of 1,5-dioxocanes via the two-fold C-O bond forming nucleophilic 4 + 4-cyclodimerization of cycloprop-2-en-1-ylmethanols // RSC Advances. - 2015. - Volume 5. - Issue 88. - Pages 71849-71853ru
dc.identifier.urihttps://www.scopus.com/record/display.uri?eid=2-s2.0-84940491140&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=dc7f8c6f40c1112203ece798567bdeb2&sot=afnl&sdt=cl&cluster=scopubyr%2c%222015%22%2ct&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&relpos=18&citeCnt=8&searchTerm=-
dc.identifier.urihttp://hdl.handle.net/20.500.12258/3699-
dc.description.abstractAn efficient [4 + 4] cyclodimerization of cyclopropenemethanols operating via a two-fold strain release-driven addition of alkoxides across the double bond of cyclopropenes was investigated. This chemo- and diastereoselective transformation provided previously unknown 2,7-dioxatricyclo[7.1.0.04,6]decane scaffoldsru
dc.language.isoenru
dc.publisherRoyal Society of Chemistryru
dc.relation.ispartofseriesRSC Advances-
dc.subjectAlkoxidesru
dc.subjectBond formingru
dc.subjectCyclodimerizationru
dc.subjectCyclopropenesru
dc.subjectDiastereoselectiveru
dc.subjectDouble bondsru
dc.subjectStrain releaseru
dc.subjectScaffoldsru
dc.titleSynthesis of 1,5-dioxocanes via the two-fold C-O bond forming nucleophilic 4 + 4-cyclodimerization of cycloprop-2-en-1-ylmethanolsru
dc.typeСтатьяru
vkr.amountPages 71849-71853ru
vkr.instИнститут математики и естественных наук-
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