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dc.contributor.authorWu, HJen_US
dc.contributor.authorTsai, SHen_US
dc.contributor.authorChung, WSen_US
dc.date.accessioned2014-12-08T15:02:50Z-
dc.date.available2014-12-08T15:02:50Z-
dc.date.issued1996-02-07en_US
dc.identifier.issn1359-7345en_US
dc.identifier.urihttp://dx.doi.org/10.1039/cc9960000375en_US
dc.identifier.urihttp://hdl.handle.net/11536/1454-
dc.description.abstractTreatment of the bis-endo-thioester and acyl group substituted norbornenes 1a-d and 9a-c with iodine in aqueous tetrahydrofuran at 25 degrees C gave the novel iodo-cage compounds 2a-d and 10a-c in 80-90% yields respectively, the first example of sequential cyclization of norbornene derivatives induced by an iodine electrophile.en_US
dc.language.isoen_USen_US
dc.titleA novel iodine-induced sequential cyclization reaction of norbornene derivatives leading to the formation of novel iodo-cage compoundsen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/cc9960000375en_US
dc.identifier.journalCHEMICAL COMMUNICATIONSen_US
dc.citation.volumeen_US
dc.citation.issue3en_US
dc.citation.spage375en_US
dc.citation.epage376en_US
dc.contributor.department交大名義發表zh_TW
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentNational Chiao Tung Universityen_US
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:A1996UG03800045-
dc.citation.woscount4-
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