Please use this identifier to cite or link to this item: https://doi.org/10.1039/c2ob06840k
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dc.titleScope of direct arylation of fluorinated aromatics with aryl sulfonates
dc.contributor.authorChang, J.W.W.
dc.contributor.authorChia, E.Y.
dc.contributor.authorChai, C.L.L.
dc.contributor.authorSeayad, J.
dc.date.accessioned2014-10-29T01:58:18Z
dc.date.available2014-10-29T01:58:18Z
dc.date.issued2012-03-21
dc.identifier.citationChang, J.W.W., Chia, E.Y., Chai, C.L.L., Seayad, J. (2012-03-21). Scope of direct arylation of fluorinated aromatics with aryl sulfonates. Organic and Biomolecular Chemistry 10 (11) : 2289-2299. ScholarBank@NUS Repository. https://doi.org/10.1039/c2ob06840k
dc.identifier.issn14770520
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/106322
dc.description.abstractThe scope and limitations of direct arylation of fluorinated aromatics with aryl sulfonates was examined. Pd(OAc) 2, in the presence of MePhos and KOAc in THF, efficiently catalyzed the direct arylation of fluoro aromatics with aryl triflates under ambient conditions. Sterically hindered triflates and heteroaryl triflates gave good to excellent yields of the cross coupled products using a modified catalyst system which involves Pd(OAc) 2-RuPhos at 100°C. The direct arylation of electron deficient arenes with aryl mesylates is also established using Pd(OAc) 2-SPhos as the catalyst in toluene- tBuOH at 120°C. © The Royal Society of Chemistry 2012.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c2ob06840k
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentPHARMACY
dc.description.doi10.1039/c2ob06840k
dc.description.sourcetitleOrganic and Biomolecular Chemistry
dc.description.volume10
dc.description.issue11
dc.description.page2289-2299
dc.description.codenOBCRA
dc.identifier.isiut000300656600016
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