3698-47-3Relevant academic research and scientific papers
Iridium-catalyzed enantioselective intramolecular hydroarylation of allylic aryl ethers devoid of a directing group on the aryl group
Kusaka, Satoshi,Ohmura, Toshimichi,Suginome, Michinori
supporting information, p. 13542 - 13545 (2021/12/23)
Although intramolecular hydroarylation is an attractive transformation of allylic aryl ethers, it has suffered from narrow substrate scope. We herein describe Ir/(S)-DTBM-SEGPHOS-catalyzed intramolecular hydroarylation of allylic aryl ethers. The reaction
Synthesis and structure of [Ru(PPh3)2(bipy)(MeCN)Cl][BPh4] and it's catalytic property towards regioselective and stereoselective allylation of phenols
Sinha, Abhilasha,Khatua, Snehadrinarayan,Bhattacharjee, Manish
supporting information, p. 116 - 120 (2015/02/19)
The compound, [Ru(PPh3)2(bipy)(MeCN)Cl][BPh4] (1) has been synthesized from the precursor complex, [Ru(bipy)(PPh3)2Cl2]. The complex has been structurally characterized. This complex has been found to be an efficient catalyst for the regioselective allylation of phenols.
ONE-POT SYNTHESES OF 2,3-DIHYDRO-2,2-DIMETHYLBENZOFURAN DERIVATIVES
Kim, Kyoung Mahn,Kim, Hyoung Rae,Ryu, Eung K.
, p. 497 - 505 (2007/10/02)
A tandem Claisen rearrangement-cyclization reaction of aryl methallyl ethers afforded the corresponding 2,3-dihydro-2,2-dimethylbenzofuran derivatives at -70 deg C with aluminium chloride.
