Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/101625
| Title: | Modular synthesis of propargylamine modified cyclodextrins by a gold(III)-catalyzed three-component coupling reaction | Authors: | Hui, TW Cui, JF Wong, MK |
Issue Date: | 2017 | Source: | RSC advances, 2017, v. 7, no. 24, p. 14477-14480 | Abstract: | An efficient modular approach for the synthesis of propargylamine modified β-cyclodextrins has been developed. Using mono-(6-benzylamino-6-deoxy)-β-cyclodextrins, formaldehyde, and alkynes, mono-(6-(benzylpropargyl)amino-6-deoxy)-β-cyclodextrins have been synthesized through a three-component coupling reaction catalyzed by gold(III) salt in water at 40 °C. | Publisher: | Royal Society of Chemistry | Journal: | RSC advances | EISSN: | 2046-2069 | DOI: | 10.1039/c7ra00249a | 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 Hui, T. W., Cui, J. F., & Wong, M. K. (2017). Modular synthesis of propargylamine modified cyclodextrins by a gold (III)-catalyzed three-component coupling reaction. RSC advances, 7(24), 14477-14480 is available at https://doi.org/10.1039/C7RA00249A. |
| Appears in Collections: | Journal/Magazine Article |
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| c7ra00249a.pdf | 662.07 kB | Adobe PDF | View/Open |
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