1443418-80-1Relevant articles and documents
Electrochemical C-H phosphorylation of 2-phenylpyridine in the presence of palladium salts
Dudkina,Gryaznova,Kataeva,Budnikova,Sinyashin
, p. 2641 - 2646 (2014)
A new approach was developed to the introduction of the phosphonate group into arylpyridines using 2-phenylpyridine as an example. The approach is the electrochemical oxidation of a mixture of 2-phenylpyridine, diethyl phosphite, and palladium acetate at room temperature. An intermediate dipalladium cyclic complex was isolated that is formed by the ortho-palladation of 2-phenylpyridine and substitution of acetate ions by phosphonate ions. The preparative oxidation of this complex selectively results in the product of the phosphorylation of the C-H bond in 2-phenylpyridine.
Pyridine-directed palladium-catalyzed electrochemical phosphonation of C(sp2)-H bond
Grayaznova, Tatyana Vasilevna,Dudkina, Yu.B.,Islamov,Kataeva,Sinyashin,Vicic,Budnikova, Yu.H.
, p. 68 - 71 (2015)
A new electrocatalytic method for the phosphonation of 2-phenylpyridine was developed. The joint electrochemical oxidation of a mixture of palladium acetate, 2-phenylpyridine, and H-diethylphosphonate affords the ortho C-H phosphonation product. The elect
Pd(II)-catalyzed phosphorylation of aryl C-H bonds
Feng, Chen-Guo,Ye, Mengchun,Xiao, Kai-Jiong,Li, Suhua,Yu, Jin-Quan
supporting information, p. 9322 - 9325 (2013/07/19)
A Pd(II)-catalyzed C-H phosphorylation reaction has been developed using heterocycle-directed ortho-palladation. Both H-phosphonates and diaryl phosphine oxides are suitable coupling partners for this reaction.