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dc.contributor.authorZhang, Wen-Zhenen_US
dc.contributor.authorMa, Huien_US
dc.contributor.authorXiang, Guang-Yaen_US
dc.contributor.authorLuo, Junen_US
dc.contributor.authorChung, Wen-Shengen_US
dc.date.accessioned2017-04-21T06:55:30Z-
dc.date.available2017-04-21T06:55:30Z-
dc.date.issued2016-07-01en_US
dc.identifier.issn2365-6549en_US
dc.identifier.urihttp://dx.doi.org/10.1002/slct.201600709en_US
dc.identifier.urihttp://hdl.handle.net/11536/133365-
dc.description.abstractCalix[4]arene diastereomeric pairs with combined axial chirality and inherent chirality were readily synthesized via monoalkylation of 1,2-substituted calix[4]arene crown-4 incorporating an axially chiral binaphthyl moiety with different electrophiles as a key step. The reaction showed high generality and distinct diastereoselectivity. The easy separation of the diaster-eomers, the good diastereoselectivity of the reaction, and the poor stereoselectivity of the chiral recognition of diastereomeric pairs were attributed to the remarkable steric effect of the axially chiral binaphthyl moiety. Absolute configurations were determined by X-ray crystallography.en_US
dc.language.isoen_USen_US
dc.subjectSupramolecular chemistryen_US
dc.subjectCalixarenesen_US
dc.subjectChiralityen_US
dc.subjectDiastereoselectivityen_US
dc.subjectMolecular recognitionen_US
dc.titleCalix[4]arenes with Combined Axial Chirality and Inherent Chirality: Synthesis, Absolute Configuration and Chiral Recognitionen_US
dc.identifier.doi10.1002/slct.201600709en_US
dc.identifier.journalCHEMISTRYSELECTen_US
dc.citation.volume1en_US
dc.citation.issue10en_US
dc.citation.spage2486en_US
dc.citation.epage2491en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000395417800061en_US
Appears in Collections:Articles