Palladium-Catalyzed Phosphorylation of Aryl Mesylates and Tosylates
作者:Wai Chung Fu、Chau Ming So、Fuk Yee Kwong
DOI:10.1021/acs.orglett.5b03104
日期:2015.12.4
The first general palladium catalyst for the phosphorylation of arylmesylates 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
anodic oxidation proceeds either via phosphiniumradicalcations, which then attack the arenes electrophilically, or via arene radicalcations, which add the trialkylphosphite as nucleophile. Aryl phosphonates are also obtained in good yield by chemical oxidation with peroxodisulfate/AgNO3 in acetonitrile/water or glacial acetic acid. The diethylphosphinium radicalcation, formed from diethylphosphite by