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dc.contributor.authorShiao, Ya-Jiunen_US
dc.contributor.authorChiang, Pei-Chenen_US
dc.contributor.authorSenthilvelan, Annamalaien_US
dc.contributor.authorTsai, Ming-Tsungen_US
dc.contributor.authorLee, Gene-Hsiangen_US
dc.contributor.authorChung, Wen-Shengen_US
dc.date.accessioned2014-12-08T15:15:22Z-
dc.date.available2014-12-08T15:15:22Z-
dc.date.issued2006-11-20en_US
dc.identifier.issn0040-4039en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.tetlet.2006.09.070en_US
dc.identifier.urihttp://hdl.handle.net/11536/11535-
dc.description.abstract1, 3-Dipolar cycloadditions of upper- and lower-rim diallylcalix[4]arenes (1 and 3) with aryl dinitrile oxides provide a unique and efficient way of capping the calix[4]arenes. When dinitrile oxides reacted with 5-allylcalix[4]arene 7, they underwent a 1,3-dipolar cycloaddition on one side and an electrophilic substitution on the other side, which led to a novel type of asymmetric calix[4]arenes (9 and 12). (c) 2006 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subject1,3-dipolar cycloadditionen_US
dc.subjectisoxazolinesen_US
dc.subjectelectrophilic substitutionen_US
dc.subjectasymmetric calix[4]arenesen_US
dc.titleCapping the upper and lower rims of calix[4]arenes by aryl dinitrile oxide reactionsen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.tetlet.2006.09.070en_US
dc.identifier.journalTETRAHEDRON LETTERSen_US
dc.citation.volume47en_US
dc.citation.issue47en_US
dc.citation.spage8383en_US
dc.citation.epage8386en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000241910200042-
dc.citation.woscount18-
Appears in Collections:Articles


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