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dc.contributor.authorTsai, Chia-Chenen_US
dc.contributor.authorHo, I-Tingen_US
dc.contributor.authorChu, Jean-Hoen_US
dc.contributor.authorShen, Li-Chingen_US
dc.contributor.authorHuang, Shou-Lingen_US
dc.contributor.authorChung, Wen-Shengen_US
dc.date.accessioned2014-12-08T15:21:51Z-
dc.date.available2014-12-08T15:21:51Z-
dc.date.issued2012-03-02en_US
dc.identifier.issn0022-3263en_US
dc.identifier.urihttp://dx.doi.org/10.1021/jo2024784en_US
dc.identifier.urihttp://hdl.handle.net/11536/15559-
dc.description.abstractAn efficient synthetic pathway for the synthesis of biscalix[4]arenes 5-10 using 1,3-dipolar cycloaddition reactions is reported. Biscalix[4]arene 10 is capable of forming a complex with methyl viologen because of favorable cation-pi interactions and a proper cavity size to accommodate the guest. Moreover, biscalix[4]arenes 8a and 8b were found to be atropisomers at room temperature. These two conformers were unable to exchange at room temperature because of the restricted rotation of the C-9-C-11 or C-10-C-12 bonds of the beta-amino-alpha,beta-unsaturated ketones of anthracene.en_US
dc.language.isoen_USen_US
dc.titleSynthesis of 9,10-Bis-ketoenaminoanthryl and 9,10-Bisi-isoxazolylanthryl Linked Biscalix[4]arenes: Atropisomers and Molecular Recognitionsen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/jo2024784en_US
dc.identifier.journalJOURNAL OF ORGANIC CHEMISTRYen_US
dc.citation.volume77en_US
dc.citation.issue5en_US
dc.citation.spage2254en_US
dc.citation.epage2262en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000300915900018-
dc.citation.woscount7-
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