Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/71413
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dc.contributor.authorElango, S.en_US
dc.contributor.authorYan, T.H.en_US
dc.date2002zh_TW
dc.date.accessioned2014-06-11T06:01:20Z-
dc.date.available2014-06-11T06:01:20Z-
dc.identifier.issn0040-4020zh_TW
dc.identifier.urihttp://hdl.handle.net/11455/71413-
dc.description.abstractA short synthesis of (+)-lycoricidine outlined herein has been accomplished by combining asymmetric chloronitroso cycloaddition with controlled installation of the bromohydrin unit, base-promoted epoxide formation, and SnCl4-catalyzed arene-epoxide cyclization. (C) 2002 Elsevier Science Ltd. All rights reserved.en_US
dc.language.isoen_USzh_TW
dc.relationTetrahedronen_US
dc.relation.ispartofseriesTetrahedron, Volume 58, Issue 36, Page(s) 7335-7338.en_US
dc.relation.urihttp://dx.doi.org/10.1016/s0040-4020(02)00736-6en_US
dc.subjectbromohydrinen_US
dc.subjectcycloadditionen_US
dc.subjectantineoplastic agentsen_US
dc.subjectd-glucoseen_US
dc.subjectaromaticsen_US
dc.titleA short synthesis of (+)-lycoricidineen_US
dc.typeJournal Articlezh_TW
dc.identifier.doi10.1016/s0040-4020(02)00736-6zh_TW
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