Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/62309
Title: Palladium(II)-catalyzed switchable mono-/diselenylation of arenes controlled by solvent effects
Authors: Jin, W
Zheng, P
Law, GL 
Wong, WT 
Keywords: Organic selenides
Selenylation
Palladium
Solvent effects
Issue Date: 2016
Publisher: Elsevier
Source: Journal of organometallic chemistry, 2016, v. 812, p. 66-73 How to cite?
Journal: Journal of organometallic chemistry 
Abstract: Organic selenides were efficient regioselective synthesized by palladium-catalyzed switchable mono and diselenylation of arenes sp(2) C-H bonds through simply tuning the DMSO to water ratio. The present protocol was also successfully extended to the monoselenylation of 2-phenoxypyridines, which bore a removable directing group, in modest yields.
URI: http://hdl.handle.net/10397/62309
ISSN: 0022-328X
DOI: 10.1016/j.jorganchem.2015.09.040
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