25994-02-9Relevant articles and documents
Dual photoredox/palladium-catalyzed C-H acylation of 2-arylpyridines with oxime esters
He, Bin-Qing,Gao, Yuan,Wang, Peng-Zi,Wu, Hong,Zhou, Hong-Bin,Liu, Xiao-Peng,Chen, Jia-Rong
supporting information, p. 373 - 377 (2020/09/11)
An unprecedented dual photoredox/palladium-catalyzed iminyl-radical-mediated C-C bond cleavage and directed ortho C-H acylation of 2-arylpyridines by using oxime esters is described. Oxime esters can serve as efficient acyl sources through formation of the corresponding acyl radicals by photoredox-catalyzed iminyl-radical-mediated C-C bond cleavage. This redox-neutral protocol features excellent regioselectivity, a broad substrate scope, and good functional-group tolerance with respect to both components, giving a broad range of aryl ketones with generally good yields.
Extraction and spectrophotometric determination of palladium(H) with 1-phenyl-1,2-butanedione dioxime
Tejam,Thakkar
, p. 364 - 366 (2007/10/03)
Extraction and spectrophotometric determination of palladium(II) has been carried out using a new reagent 1-phenyl-1,2-butanedione dioxime (H2PBDD) which forms a yellow coloured complex with Pd(II). The complex can be quantitatively extracted i