39880-81-4Relevant articles and documents
Tetraethylammonium iodide catalyzed synthesis of diaryl ketones via the merger of cleavage of C-C double bonds and recombination of aromatic groups
Zeng, Xianghua,Xu, Daqian,Miao, Chengxia,Xia, Chungu,Sun, Wei
, p. 46494 - 46497 (2014/12/10)
An efficient method for synthesizing diaryl ketones via merging of oxidative cleavage of C-C double bonds and recombination of aromatic groups is developed with Et4NI (2.5 mol%) as the catalyst and NaIO4 as the oxidant. The control experiments provide valuable mechanistic insights into the formation of diaryl ketones, and suggest that NaIO4 serves as an epoxidation and nucleophilic deformylation reagent.
Platelet antiaggregant methoxyphenylthienyl ketoxime ethers: Synthesis and structure-activity relationships
Varache-Lembege,Nuhrich,Renard,Duboudin,Vercauteren,Devaux
, p. 417 - 424 (2007/10/02)
Some new oximinoalkanoic (n = 2,3,4) esters and acids derived from methoxyphenylthienyl ketones have been synthesized and evaluated in vitro for their inhibitory effects on arachidonic acid-induced human platelet aggregation. Of the eighteen oximinoethers