Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/43956
Title: Palladium-catalyzed phosphorylation of aryl mesylates and tosylates
Authors: Fu, WC
So, CM
Kwong, FY 
Issue Date: 2015
Publisher: American Chemical Society
Source: Organic letters, 2015, v. 17, no. 23, p. 5906-5909 How to cite?
Journal: Organic letters 
Abstract: The first general palladium catalyst for the phosphorylation of aryl mesylates and tosylates is reported. The newly developed system exhibits excellent functional group compatibility. For instance, free amino, keto, ester, and amido groups, as well as heterocycles, remain intact during the course of reaction. The mesylated derivatives of biologically active compounds such as 17β-estradiol and 6-hydroxyflavone are also shown to be applicable substrates. A one-pot phosphorylation-amination sequence is described for the facile synthesis of potential pharmacophores.
URI: http://hdl.handle.net/10397/43956
ISSN: 1523-7060
EISSN: 1523-7052
DOI: 10.1021/acs.orglett.5b03104
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