51864-08-5Relevant articles and documents
Low-dose paeonol derivatives alleviate lipid accumulation
Pao, Kuan-Chuan,Zhao, Jin-Feng,Lee, Tzong-Shyuan,Huang, Ying-Pei,Han, Chien-Chung,Sherlock Huang, Lin-Chiang,Wu, Kou-Hung,Hsu, Ming-Hua
, p. 5652 - 5656 (2015/03/04)
Here, we present a series of novel paeonol derivatives that prevent lipid accumulation at lower doses and exhibit improved water solubility. According to SAR analysis results, 1-(4-methoxy-2-(2-(piperidin-1-yl)ethoxy)phenyl)ethanone (6a) and 4′-methoxy-2′
Synthesis of 1,2-benzisoxazole 2-oxides
Kociolek, Martin G.,Hoermann, Olivia
body text, p. 2632 - 2638 (2012/08/08)
(Chemical Equation Presented) A series of 2-hydroxyaryl ketoximes were converted to the corresponding 1,2- benzisoxazole 2-oxides by treatment with iodobenzene diacetate (in acetic acid or methanol) or N-chlorosuccinimide in water. Both methods gave moderate to excellent yields for a variety of substituted oximes under mild conditions within short reaction times. The latter method has the advantages of an aqueous solvent and lack of halogenated organic by-products. Copyright Taylor & Francis Group, LLC.
Microwave-assisted efficient one-step synthesis of amides from ketones and benzoxazoles from (2-hydroxyaryl) ketones with acetohydroxamic acid using sulfuric acid as the catalyst
Madabhushi, Sridhar,Chinthala, Narsaiah,Vangipuram, Venkata Sairam,Godala, Kondal Reddy,Jillella, Raveendra,Mallu, Kishore Kumar Reddy,Beeram, China Ramanaiah
experimental part, p. 6103 - 6107 (2011/11/30)
Efficient one-step method for the synthesis of amides directly from ketones and benzoxazoles from (2-hydroxyaryl) ketones by the reaction of acetohydroxamic acid using sulfuric acid as catalyst was described.