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dc.contributor.authorTan, Daniel
dc.contributor.authorMassera, C.
dc.contributor.authorMocerino, Mauro
dc.date.accessioned2020-08-02T08:33:46Z
dc.date.available2020-08-02T08:33:46Z
dc.date.issued2019
dc.identifier.citationTan, D.A. and Massera, C. and Mocerino, M. 2019. Partial functionalisation of C4-symmetric tetramethoxyresorcinarenes. Supramolecular Chemistry. 31 (7): pp. 442-450.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/80332
dc.identifier.doi10.1080/10610278.2019.1620949
dc.description.abstract

© 2019 Informa UK Limited, trading as Taylor & Francis Group. Investigations into the distal-functionalisation of the phenols of racemic C4-symmetric tetramethoxyresorcinarene has led to a simple, single-step procedure that allows the isolation of gram quantities of partially silylated derivatives, with the targeted distally silylated resorcinarene being obtained in a yield of 31%. These partially silylated derivatives would serve as versatile intermediates for the selective functionalisation of this elegant architecture. The solid-state structures of many of these derivatives have been determined by single crystal X-ray crystallography.

dc.languageEnglish
dc.publisherTAYLOR & FRANCIS LTD
dc.subjectScience & Technology
dc.subjectPhysical Sciences
dc.subjectChemistry, Multidisciplinary
dc.subjectChemistry
dc.subjectResorcinarene
dc.subjectcalixarene
dc.subjectaxially chiral
dc.subjectselective functionalisation
dc.subjectCHIRAL CALIXARENES SYNTHESIS
dc.subjectENANTIOMERICALLY PURE
dc.subjectRECOGNITION
dc.titlePartial functionalisation of C4-symmetric tetramethoxyresorcinarenes
dc.typeJournal Article
dcterms.source.volume31
dcterms.source.number7
dcterms.source.startPage442
dcterms.source.endPage450
dcterms.source.issn1061-0278
dcterms.source.titleSupramolecular Chemistry
dc.date.updated2020-08-02T08:33:45Z
curtin.note

This is an accepted manuscript of an article published by Taylor & Francis in Supramolecular Chemistry on 30/05/2019 available online at http://www.tandfonline.com/10.1080/10610278.2019.1620949.

curtin.departmentSchool of Molecular and Life Sciences (MLS)
curtin.accessStatusOpen access
curtin.facultyFaculty of Science and Engineering
curtin.contributor.orcidMocerino, Mauro [0000-0001-9514-7846]
curtin.contributor.researcheridMocerino, Mauro [B-2793-2011]
dcterms.source.eissn1029-0478
curtin.contributor.scopusauthoridMocerino, Mauro [6603180005]


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