Please use this identifier to cite or link to this item:
|Title:||Scope of direct arylation of fluorinated aromatics with aryl sulfonates|
|Citation:||Chang, 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|
|Abstract:||The 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.|
|Source Title:||Organic and Biomolecular Chemistry|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Feb 14, 2019
WEB OF SCIENCETM
checked on Jan 29, 2019
checked on Oct 5, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.