完整後設資料紀錄
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dc.contributor.authorShu, CMen_US
dc.contributor.authorLin, WLen_US
dc.contributor.authorLee, GHen_US
dc.contributor.authorPeng, SMen_US
dc.contributor.authorChung, WSen_US
dc.date.accessioned2014-12-08T15:45:43Z-
dc.date.available2014-12-08T15:45:43Z-
dc.date.issued2000-02-01en_US
dc.identifier.issn0009-4536en_US
dc.identifier.urihttp://hdl.handle.net/11536/30751-
dc.description.abstractThe upper rim substituted mono- and diisoxazolinomethylcalix[4]arenes 9-23 are synthesized in good yields from 1,3-dipolar cycloaddition reactions of para-substituted phenyl nitrileoxides with 5-allyl-, 5,11-diallyl- and 5,17-diallycalix[4]arenes 5-7; the structures of 9-23 are consistent with a 'cone' conformation and the 'vase-with-a-lid' structure of 11 was confirmed by a single-crystal x-ray analysis. Preliminary results show that the monoisoxazolinomethylcalix[4]arene can form an inclusion complex with ammonium cation.en_US
dc.language.isoen_USen_US
dc.subject1,3-dipolaren_US
dc.subjectcalix[4]areneen_US
dc.subjectisoxazolineen_US
dc.subjectnitrile oxidesen_US
dc.subjectClaisen rearrangementen_US
dc.titleCalix[4]arenes with a lid in their upper rims: 1,3-dipolar cycloaddition reactions of benzonitrile oxides with 5-allyl-, 5,11-dially- and 5,17-diallylcalix[4]arenesen_US
dc.typeArticleen_US
dc.identifier.journalJOURNAL OF THE CHINESE CHEMICAL SOCIETYen_US
dc.citation.volume47en_US
dc.citation.issue1en_US
dc.citation.spage173en_US
dc.citation.epage182en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000085946500020-
dc.citation.woscount13-
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