Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/103522
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dc.contributor.authorChan, Philip Wai Hongen
dc.contributor.authorTejo, Ciputraen
dc.contributor.authorSim, Xiao Rongen
dc.contributor.authorLee, Bo Raen
dc.contributor.authorAyers, Benjamin Jamesen
dc.contributor.authorLeung, Chung-Hangen
dc.contributor.authorMa, Dik-Lungen
dc.date.accessioned2015-10-01T07:46:11Zen
dc.date.accessioned2019-12-06T21:14:29Z-
dc.date.available2015-10-01T07:46:11Zen
dc.date.available2019-12-06T21:14:29Z-
dc.date.copyright2015en
dc.date.issued2015en
dc.identifier.citationTejo, C., Sim, X., Lee, B., Ayers, B., Leung, C. H., Ma, D. L., et al. (2015). Iminoiodane- and Brønsted Base-Mediated Cross Dehydrogenative Coupling of Cyclic Ethers with 1,3-Dicarbonyl Compounds. Molecules, 20(7), 13336-13353.en
dc.identifier.issn1420-3049en
dc.identifier.urihttps://hdl.handle.net/10356/103522-
dc.description.abstractA one-pot, two-step approach to prepare 2-tetrahydrofuran and -pyran substituted 1,3-dicarbonyl compounds by PhI=NTs-mediated amination/Brønsted base-catalyzed cross dehydrogenative coupling (CDC) reaction of the cyclic ether and 1,3-dicarbonyl derivative under mild conditions is reported. The reaction is compatible with a variety of cyclic ethers and 1,3-dicarbonyl compounds, affording the corresponding coupled products in moderate to good yields of up to 80% over two steps.en
dc.language.isoenen
dc.relation.ispartofseriesMoleculesen
dc.rights© 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).en
dc.titleIminoiodane- and Brønsted Base-Mediated Cross Dehydrogenative Coupling of Cyclic Ethers with 1,3-Dicarbonyl Compoundsen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen
dc.identifier.doi10.3390/molecules200713336en
dc.description.versionPublished versionen
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