Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/101625
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dc.contributorMainland Development Officeen_US
dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.creatorHui, TWen_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/10397/101625-
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 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.en_US
dc.titleModular synthesis of propargylamine modified cyclodextrins by a gold(III)-catalyzed three-component coupling reactionen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage14477en_US
dc.identifier.epage14480en_US
dc.identifier.volume7en_US
dc.identifier.issue24en_US
dc.identifier.doi10.1039/c7ra00249aen_US
dcterms.abstractAn 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.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationRSC advances, 2017, v. 7, no. 24, p. 14477-14480en_US
dcterms.isPartOfRSC advancesen_US
dcterms.issued2017-
dc.identifier.scopus2-s2.0-85014847861-
dc.identifier.eissn2046-2069en_US
dc.description.validate202308 bckwen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberABCT-0828-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China; The Hong Kong Polytechnic University; State Key Laboratory of Chirosciencesen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS6729466-
dc.description.oaCategoryCCen_US
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