Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/101626
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Title: Selective C-H bond hydroxylation of cyclohexanes in water by supramolecular control
Authors: Yang, B 
Cui, JF 
Wong, MK 
Issue Date: 2017
Source: RSC advances, 2017, v. 7, no. 49, p. 30886-30893
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.
Publisher: Royal Society of Chemistry
Journal: RSC advances 
EISSN: 2046-2069
DOI: 10.1039/c7ra03930a
Rights: This journal is © The Royal Society of Chemistry 2017
This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence (https://creativecommons.org/licenses/by-nc/3.0/).
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.
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