836-38-4Relevant academic research and scientific papers
2-Pyridylmethyl ether: A readily removable and efficient directing group for amino acid ligand accelerated ortho-C-H olefination of phenols
Cong, Xuefeng,You, Jingsong,Gao, Ge,Lan, Jingbo
supporting information, p. 662 - 664 (2013/02/25)
2-Pyridylmethyl ether-directed ortho-C-H olefination of phenols via a seven-membered cyclopalladated intermediate has been disclosed to construct a variety of ortho-alkenyl phenols and ortho-alkyl phenols.
Highly Efficient and Convenient Methods for the Direct Conversion of Aryl Silyl Ethers and Aryl Acetates into Aryl Alkyl Ethers
Oriyama, Takeshi,Noda, Kojiro,Yatabe, Kaori
, p. 701 - 703 (2007/10/03)
Direct conversion of aryl trialkylsilyl ethers and aryl acetates into the corresponding alkyl-protected phenols such as benzyl and allyl ethers can be conveniently performed by the reaction with alkyl halide in the presence of cesium fluoride and sodium methoxide, respectively, in a one-pot procedure.
Hypolipidemic analogues of ethyl 4 benzyloxybenzoate
Baggaley,Fears,Hindley,Morgan,Murrell,Thorne
, p. 1388 - 1393 (2007/10/05)
A series of compounds related to ethyl 4-benzyloxybenzoate was synthesized and evaluated for potential hypolipidemic activity in rats. Structure-activity relationships are discussed in terms of cholesterol-lowering activity together with effects on body weight gain and liver lipids. A number of the compounds inhibited cholesterol and free fatty acid biosynthesis from [1-14C]acetate in rat liver slices in vitro. Ethyl 4-benzyloxybenzoate, ethyl 4-benzyloxybenzoic acid, ethyl 4-p-bromobenzyloxybenzoate, and ethyl 4-o-methoxybenzyloxyphenyl acetate exhibited the most favorable spectrum of activity.
