Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/85008
DC FieldValueLanguage
dc.creatorWen-Hua Chiouen_US
dc.creatorChien-Lun Kaoen_US
dc.creatorJui-Chi Tsaien_US
dc.creatorYun-Man Changen_US
dc.date2013zh_TW
dc.date.accessioned2014-11-26T08:49:14Z-
dc.date.available2014-11-26T08:49:14Z-
dc.identifier.urihttp://hdl.handle.net/11455/85008-
dc.description.abstractA parallel, versatile and efficient route to synthesis of pyrrolidinoindoline and tetrahydrofuranoindoline alkaloids from cinnamyl derivatives has been developed, featuring a domino Rh-catalyzed hydroformylation–double cyclization sequence. This method can be applied to the syntheses of anti-Alzheimer drugs such as physostigmine and physovenine.en_US
dc.format.medium期刊論文zh_TW
dc.language.isoen_USzh_TW
dc.relationChem. Commun., Volume49, Page(s) 8232-8234.en_US
dc.relation.urihttp://pubs.rsc.org/en/Content/ArticleLanding/2013/CC/c3cc43257b#!divAbstractzh_TW
dc.titleDomino Rh-catalyzed hydroformylation–doublecyclization of o-amino cinnamyl derivatives:applications to the formal total syntheses ofphysostigmine and physovenineen_US
dc.identifier.doi10.1039/C3CC43257Bzh_TW
item.languageiso639-1en_US-
item.grantfulltextrestricted-
item.fulltextwith fulltext-
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