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dc.contributor.authorEdwards, Andrew
dc.contributor.authorBennin, Trevor
dc.contributor.authorRubina, Marina
dc.contributor.authorRubin, Michael
dc.identifier.citationEdwards, A., Bennin, T., Rubina, M., & Rubin, M. (2015). 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, 5(88), 71849–71853.
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[,6]decane scaffolds.en_US
dc.publisherRoyal Society of Chemistryen_US
dc.titleSynthesis of 1,5-Dioxocanes via the Two-Fold C-O Bond Forming Nucleophilic 4+4-Cyclodimerization of Cycloprop-2-en-1-ylmethanolsen_US
kusw.kuauthorEdwards, Andrew
kusw.kuauthorBennin, Trevor
kusw.kuauthorRubina, Marina
kusw.kuauthorRubin, Michael
dcterms.rightsThis is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License 4.0 (CC BY-NC-ND 4.0), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
kusw.oaversionScholarly/refereed, publisher versionen_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US

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