Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/85000
DC FieldValueLanguage
dc.creatorHuei-Lin Chuangen_US
dc.creatorR. C. Sawanten_US
dc.creatorShun-Yuan Luoen_US
dc.date2013zh_TW
dc.date.accessioned2014-11-26T08:42:23Z-
dc.date.available2014-11-26T08:42:23Z-
dc.identifier.urihttp://hdl.handle.net/11455/85000-
dc.description.abstractA d-talose derivative underwent unexpected cyclization during a Mitsunobu reaction. A plausible pathway for the reaction involves an attack of the nucleophilic azide on the benzyl ring by intramolecular cyclization with loss of the benzyl group. These newly formed, unexpected compounds may be used in the synthesis of ­derivatives of C-nucleosides.en_US
dc.format.medium期刊論文zh_TW
dc.language.isoen_USzh_TW
dc.relationSynlett, Volume 24, Issue 4, Page(s) 522-526.en_US
dc.relation.urihttps://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0032-1318196-
dc.subjectMitsunobu reactionen_US
dc.subjecttetrahydroxyen_US
dc.subjectLCBen_US
dc.subjectden_US
dc.subjecttaloseen_US
dc.subject­nucleosidesen_US
dc.subjectcyclizationen_US
dc.titleUnexpected Cyclization During the Mitsunobu Reaction of d-Talose Derivativesen_US
dc.identifier.doi10.1055/s-0032-1318196zh_TW
item.fulltextno fulltext-
item.grantfulltextnone-
item.languageiso639-1en_US-
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