78726-16-6Relevant academic research and scientific papers
Efficient catalytic-free method to produce α-aryl cycloalkanones through highly chemoselective coupling of aryl compounds with oxyallyl cations
Luo, Juan,Zhou, Hui,Hu, Jiwei,Wang, Rui,Tang, Qiang
, p. 17370 - 17377 (2014/05/06)
Catalytic-free coupling of aryl compounds and α-halo cycloketones via in situ generated oxyallyl cation intermediates is reported here. The reactions efficiently afford α-naphthol cycloalkanones with moderate to excellent yields. Electron-rich aromatic compounds are also used to produce the corresponding α-aryl cycloalkanones, and in some cases, analytically pure products are obtained after simple filtration followed by evaporation.
Enantioselective synthesis of chiral β-aryloxy alcohols by ruthenium-catalyzed ketone hydrogenation via dynamic kinetic resolution (DKR)
Bai, Wen-Ju,Xie, Jian-Hua,Li, Ya-Li,Liu, Sheng,Zhou, Qi-Lin
supporting information; experimental part, p. 81 - 84 (2010/06/16)
A highly efficient enantioselective synthesis of chiral β-aryloxy alcohols by the [RuCl2[(S)-SDP][(R, R)-DPEN]} [(Sa,R, R)-1a; SDP = 7, 7′-bis-(diarylphosphino)-1,1′-spirobiindane; DPEN = trans-1,2-diphenylethylenediamine] complex-ca
