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dc.contributor.advisor조천규-
dc.contributor.author신형섭-
dc.date.accessioned2020-02-25T16:30:50Z-
dc.date.available2020-02-25T16:30:50Z-
dc.date.issued2015-02-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/128741-
dc.identifier.urihttp://hanyang.dcollection.net/common/orgView/200000425924en_US
dc.description.abstractWe have developed a new synthetic route to (±)-lycorine via the endo-cycloadduct of 3,5-dibromo-2-pyrone and (E)-β-borylstyrene. Boronate oxidation and a set of reactions including face-selective epoxidation provided the pivotal C1-OH group and C3/C3a double bond effectively.-
dc.publisher한양대학교-
dc.titleTotal Synthesis of (±)-Lycorine from the Endo-Cycloadduct of 3,5-Dibromo-2-pyrone and (E)-β-borylstyrene-
dc.typeTheses-
dc.contributor.googleauthor신형섭-
dc.contributor.alternativeauthorShin, Hyeong-Seob-
dc.sector.campusS-
dc.sector.daehak대학원-
dc.sector.department화학과-
dc.description.degreeMaster-
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GRADUATE SCHOOL[S](대학원) > CHEMISTRY(화학과) > Theses (Master)
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