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dc.contributor.author조천규-
dc.date.accessioned2018-03-26T07:51:37Z-
dc.date.available2018-03-26T07:51:37Z-
dc.date.issued2014-09-
dc.identifier.citationOrganic Letters, 2014, 16(21), P.5718-5720en_US
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.urihttps://pubs.acs.org/doi/abs/10.1021/ol502792p-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/52569-
dc.description.abstractA new synthetic route to (±)-lycorine, starting from the endo-cycloadduct of 3,5-dibromo-2-pyrone and (E)-β-borylstyrene, is reported. Boronate oxidation and a set of reactions including face-selective epoxidation provided the pivotal C1-OH group and C3/C3a double bond.en_US
dc.description.sponsorshipThis work was supported by the grants from the National Research Foundation of korea (2012R1A2A4A01005064 and 2012M3A7B4049661).en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectAmaryllidaceae Alkaloidsen_US
dc.subjectchemical synthesisen_US
dc.subjectMolecular Structureen_US
dc.subjectOxidation-Reductionen_US
dc.subjectPhenanthridinesen_US
dc.subjectPyronesen_US
dc.subjectchemistryen_US
dc.subjectStereoisomerismen_US
dc.subjectStyrenesen_US
dc.titleTotal Synthesis of (+/-)-Lycorine from the Endo-Cycloadduct of 3,5-Dibromo-2-pyrone and (E)-beta-Borylstyreneen_US
dc.title.alternative-)-Lycorine from the Endo-Cycloadduct of 3,5-Dibromo-2-pyrone and (E)-beta-Borylstyreneen_US
dc.typeArticleen_US
dc.relation.no21-
dc.relation.volume16-
dc.identifier.doi10.1021/ol502792p-
dc.relation.page5718-5720-
dc.relation.journalORGANIC LETTERS-
dc.contributor.googleauthorShin, Hyeong-Seob-
dc.contributor.googleauthorJung, Yong-Geun-
dc.contributor.googleauthorCho, Hyun-Kyu-
dc.contributor.googleauthorPark, Yong-Gyu-
dc.contributor.googleauthorCho, Cheon-Gyu-
dc.relation.code2014037111-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF NATURAL SCIENCES[S]-
dc.sector.departmentDEPARTMENT OF CHEMISTRY-
dc.identifier.pidccho-
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COLLEGE OF NATURAL SCIENCES[S](자연과학대학) > CHEMISTRY(화학과) > Articles
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