Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/26511
DC FieldValueLanguage
dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorWong, PY-
dc.creatorChow, WK-
dc.creatorChung, KH-
dc.creatorSo, CM-
dc.creatorLau, CP-
dc.creatorKwong, FY-
dc.date.accessioned2015-06-23T09:10:52Z-
dc.date.available2015-06-23T09:10:52Z-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/10397/26511-
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.titleA versatile palladium catalyst system for Suzuki-Miyaura coupling of alkenyl tosylates and mesylatesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage8328-
dc.identifier.epage8330-
dc.identifier.volume47-
dc.identifier.issue29-
dc.identifier.doi10.1039/c1cc12240a-
dcterms.abstractA general and effective palladium system for Suzuki-Miyaura coupling of alkenyl electrophiles under mild reaction conditions is reported. With the Pd(OAc)2/CM-phos system, a variety of alkenyl tosylates are coupled well with ArB(OH)2. Moreover, the first successful examples of using alkenyl mesylates in alkenylation are also described.-
dcterms.bibliographicCitationChemical communications, 2011, v. 47, no. 29, p. 8328-8330-
dcterms.isPartOfChemical communications-
dcterms.issued2011-
dc.identifier.isiWOS:000292980900038-
dc.identifier.scopus2-s2.0-79960432901-
dc.identifier.eissn1364-548X-
dc.identifier.rosgroupidr54660-
dc.description.ros2010-2011 > Academic research: refereed > Publication in refereed journal-
Appears in Collections:Journal/Magazine Article
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