Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/101626
| DC Field | Value | Language |
|---|---|---|
| dc.contributor | Mainland Development Office | - |
| dc.contributor | Department of Applied Biology and Chemical Technology | - |
| dc.creator | Yang, B | en_US |
| dc.creator | Cui, JF | en_US |
| dc.creator | Wong, MK | en_US |
| dc.date.accessioned | 2023-09-18T07:31:41Z | - |
| dc.date.available | 2023-09-18T07:31:41Z | - |
| dc.identifier.uri | http://hdl.handle.net/10397/101626 | - |
| dc.language.iso | en | en_US |
| dc.publisher | Royal Society of Chemistry | en_US |
| dc.rights | This journal is © The Royal Society of Chemistry 2017 | en_US |
| dc.rights | This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence (https://creativecommons.org/licenses/by-nc/3.0/). | en_US |
| dc.rights | The 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.title | Selective C-H bond hydroxylation of cyclohexanes in water by supramolecular control | en_US |
| dc.type | Journal/Magazine Article | en_US |
| dc.identifier.spage | 30886 | en_US |
| dc.identifier.epage | 30893 | en_US |
| dc.identifier.volume | 7 | en_US |
| dc.identifier.issue | 49 | en_US |
| dc.identifier.doi | 10.1039/c7ra03930a | en_US |
| dcterms.abstract | A 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.accessRights | open access | en_US |
| dcterms.bibliographicCitation | RSC advances, 2017, v. 7, no. 49, p. 30886-30893 | en_US |
| dcterms.isPartOf | RSC advances | en_US |
| dcterms.issued | 2017 | - |
| dc.identifier.scopus | 2-s2.0-85021649040 | - |
| dc.identifier.eissn | 2046-2069 | en_US |
| dc.description.validate | 202308 bckw | - |
| dc.description.oa | Version of Record | en_US |
| dc.identifier.FolderNumber | ABCT-0829 | - |
| dc.description.fundingSource | get from publ pdf | en_US |
| dc.description.fundingText | National Natural Science Foundation of China; The Hong Kong Polytechnic University; The State Key Laboratory of Chirosciences | en_US |
| dc.description.pubStatus | Published | en_US |
| dc.identifier.OPUS | 6756535 | - |
| dc.description.oaCategory | CC | en_US |
| Appears in Collections: | Journal/Magazine Article | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| c7ra03930a.pdf | 1.23 MB | Adobe PDF | View/Open |
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