Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/101626
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dc.contributorMainland Development Office-
dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorYang, Ben_US
dc.creatorCui, JFen_US
dc.creatorWong, MKen_US
dc.date.accessioned2023-09-18T07:31:41Z-
dc.date.available2023-09-18T07:31:41Z-
dc.identifier.urihttp://hdl.handle.net/10397/101626-
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.rightsThis journal is © The Royal Society of Chemistry 2017en_US
dc.rightsThis article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence (https://creativecommons.org/licenses/by-nc/3.0/).en_US
dc.rightsThe following publication Yang, B., Cui, J. F., & Wong, M. K. (2017). Selective C–H bond hydroxylation of cyclohexanes in water by supramolecular control. RSC advances, 7(49), 30886-30893 is available at https://doi.org/10.1039/C7RA03930A.en_US
dc.titleSelective C-H bond hydroxylation of cyclohexanes in water by supramolecular controlen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage30886en_US
dc.identifier.epage30893en_US
dc.identifier.volume7en_US
dc.identifier.issue49en_US
dc.identifier.doi10.1039/c7ra03930aen_US
dcterms.abstractA new approach for selective hydroxylation of non-activated cyclohexanes using dioxirane generated in situ in water through supramolecular control has been developed. Using β-CD and γ-CD as the supramolecular hosts, selective hydroxylation of cyclohexane substrates, including trans/cis-1,4-, 1,3-and 1,2-dimethylcyclohexanes and trans/cis-decahydronaphthalene, was achieved in up to 54% yield in water. Furthermore, site-selective C-H bond hydroxylation of (+)-menthol was achieved by obstructing the approach of dioxirane to the C-H bond with higher steric hindrance through inclusion complexation with β-CD and γ-CD in water.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationRSC advances, 2017, v. 7, no. 49, p. 30886-30893en_US
dcterms.isPartOfRSC advancesen_US
dcterms.issued2017-
dc.identifier.scopus2-s2.0-85021649040-
dc.identifier.eissn2046-2069en_US
dc.description.validate202308 bckw-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberABCT-0829-
dc.description.fundingSourceget from publ pdfen_US
dc.description.fundingTextNational Natural Science Foundation of China; The Hong Kong Polytechnic University; The State Key Laboratory of Chirosciencesen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS6756535-
dc.description.oaCategoryCCen_US
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