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dc.contributor.author원호식-
dc.date.accessioned2020-04-14T02:33:03Z-
dc.date.available2020-04-14T02:33:03Z-
dc.date.issued2004-06-
dc.identifier.citationJournal of Korean Magnetic Resonance Society, v. 8, No. 1, Page. 62-69en_US
dc.identifier.issn1226-6531-
dc.identifier.urihttp://www.koreascience.or.kr/article/JAKO200411922974314.page-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/150973-
dc.description.abstractBicyclolactones obtained from the Diels-Alder cycloaddition of 3,5-dibromo-2-pyrone can undergo various palladium catalyzed cross coupling reactions to afford aryl bicyclolactones. The resulting coupled products can be readily converted into various 3-OH cyclohexenes via lactone ring openings, while those bearing dienyl units underwent highly diastereoselective Diels-Alder cycloadditions with selected dienophiles to funish multiply functionalized polycarbocycles. Bromo-bicyclic diene furnished two different diastereomers endo-form (62%) and exo-form (38%) upon cycloadditions with N-Et maleimide (NEM), and their stereochemistries were identified with NMRen_US
dc.description.sponsorshipThe financial support of Hanyang University(2001) to H.W. is greatly acknowledged.en_US
dc.language.isoen_USen_US
dc.publisherKorean Magnetic Resonance Societyen_US
dc.titleNMR signal assignments of the stereochemical cycloadducts of bicyclolactone via Diels-Alder reactionen_US
dc.typeArticleen_US
dc.relation.journalJournal of Korean Magnetic Resonance Society-
dc.contributor.googleauthorKim, Dae-Sung-
dc.contributor.googleauthorSeo, Chan-Woo-
dc.contributor.googleauthorCho, Cheon-Gyu-
dc.contributor.googleauthorWon, Ho-Shik-
dc.relation.code2012205307-
dc.sector.campusE-
dc.sector.daehakCOLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY[E]-
dc.sector.departmentDEPARTMENT OF CHEMICAL AND MOLECULAR ENGINEERING-
dc.identifier.pidhswon-


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