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A Concise Total Synthesis of (±)-Mesembrine
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dc.contributor.authorKim, Hyoungsu-
dc.contributor.authorChoi, Hosam-
dc.contributor.authorLee, Kiyoun-
dc.date.issued2018-06-01-
dc.identifier.urihttps://dspace.ajou.ac.kr/dev/handle/2018.oak/30105-
dc.description.abstractA concise total synthesis of (±)-mesembrine has been successfully accomplished in seven steps and 24% overall yield from commercially available 3-ethoxy-2-cyclohexen-1-one. Central to the assembly of the skeleton of mesembrine are a Johnson-Claisen rearrangement for the formation of the benzylic quaternary stereocenter and direct allylic oxidation to generate the substrate for the amidation/transannular aza-conjugate addition reaction.-
dc.description.sponsorshipThis work was supported by the Basic Science Research Program from the National Research Foundation of Korea (NRF-2016R1C1B1008816) funded by the Ministry of Education and the 2017 Research Fund of the Catholic University of Korea.Noaitnal Reseacrh Foundoaitn of Koera N(RF-2016R1C1B1008816)-
dc.language.isoeng-
dc.publisherGeorg Thieme Verlag-
dc.titleA Concise Total Synthesis of (±)-Mesembrine-
dc.typeArticle-
dc.citation.endPage1206-
dc.citation.startPage1203-
dc.citation.titleSynlett-
dc.citation.volume29-
dc.identifier.bibliographicCitationSynlett, Vol.29, pp.1203-1206-
dc.identifier.doi10.1055/s-0036-1591547-
dc.identifier.scopusid2-s2.0-85042192991-
dc.identifier.urlhttp://www.thieme-connect.com/ejournals/toc/synlett-
dc.subject.keyword3a-(aryl)octahydro-indole-
dc.subject.keywordallylic transfer-
dc.subject.keywordbenzylic quaternary stereogenic center-
dc.subject.keywordmesembrine-
dc.subject.keywordnatural products-
dc.subject.keywordtotal synthesis-
dc.description.isoafalse-
dc.subject.subareaOrganic Chemistry-
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