Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/60997
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorYang, Q-
dc.creatorChoy, PY-
dc.creatorWu, Y-
dc.creatorFan, B-
dc.creatorKwong, FY-
dc.date.accessioned2016-12-19T08:54:19Z-
dc.date.available2016-12-19T08:54:19Z-
dc.identifier.issn1477-0520-
dc.identifier.urihttp://hdl.handle.net/10397/60997-
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.rightsThis article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence (CC BY-NC 3.0) (https://creativecommons.org/licenses/by-nc/3.0/).en_US
dc.titleOxidative coupling between C(sp2)-H and C(sp3)-H bonds of indoles and cyclic ethers/cycloalkanesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage2608-
dc.identifier.epage2612-
dc.identifier.volume14-
dc.identifier.issue9-
dc.identifier.doi10.1039/c6ob00076b-
dcterms.abstractCross-dehydrogenative-coupling (CDC) between C-H/C-H bonds of indoles and cyclic ethers/cycloalkanes is made viable through a simple transition-metal-free pathway. With the aid of only di-tert-butyl peroxide, a number of inactive cyclic ethers and cycloalkanes can be directly coupled with indole derivatives in satisfactory yields.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationOrganic & biomolecular chemistry, 2016, v. 14, no. 9, p. 2608-2612-
dcterms.isPartOfOrganic & biomolecular chemistry-
dcterms.issued2016-
dc.identifier.isiWOS:000371041500003-
dc.identifier.scopus2-s2.0-84959239208-
dc.identifier.pmid26842403-
dc.identifier.eissn1477-0539-
dc.identifier.rosgroupid2015003180-
dc.description.ros2015-2016 > Academic research: refereed > Publication in refereed journal-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRAen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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