127943-22-0Relevant articles and documents
PHENYL BENZYL ETHER DERIVATIVE AND PREPARATION METHOD AND APPLICATION THEREOF
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Paragraph 0167; 0168, (2017/06/12)
Parts of compounds, after being labeled by radionuclide, of the phenyl benzyl ether derivative, are used as Aβ plaque imaging agent. The structural formula of the phenyl benzyl ether derivative is shown by formula (I). The present invention develops a kin
Preliminary evaluation of fluoro-pegylated benzyloxybenzenes for quantification of β-amyloid plaques by positron emission tomography
Yang, Yanping,Fu, Hualong,Cui, Mengchao,Peng, Cheng,Liang, Zhigang,Dai, Jiapei,Zhang, Zhiyong,Lin, Chunping,Liu, Boli
, p. 86 - 96 (2015/10/19)
A new series of fluoro-pegylated benzyloxybenzenes were designed, synthesized and evaluated as PET probes for early detection of Aβ plaques. Molecular docking revealed that all of the flexible benzyloxybenzenes inserted themselves into the hydrophobic Val
Silica-attached molecular receptor complexes for benzoates and naphthoates
Hodyl, Jozef A.Z.,Lincoln, Stephen F.,Wainwright, Kevin P.
experimental part, p. 261 - 270 (2011/12/01)
A series of cyclen (1,4,7,10-tetraazacyclododecane) derived molecular receptors for aromatic oxoanions, that are activated by complexation with Cd(II), have been covalently linked to 3-(glycidoxy)propyl-functionalised silica gel (70-230 mesh). These immob
Translational Isomerism in Some Two- and Three-Station [2]Rotaxanes
Amabilino, David B.,Ashton, Peter R.,Boyd, Sue E.,Gomez-Lopez, Marcos,Hayes, Wayne,Stoddart, J. Fraser
, p. 3062 - 3075 (2007/10/03)
The template-directed syntheses of three [2]rotaxanes are described. They all have dumbbell , components, with both hydroquinone and resorcinol rings inserted into polyether chains terminated by tetraarylmethane stoppers, that become encircled during the key self-assembly processes by the tetracationic cyclophane, cyclobis(paraquat-p-phenylene), with its two π-electron deficient bipyridinium units. It has been demonstrated by low-temperature 1H NMR spectroscopy that the π-electron deficient tetracationic cyclophane has a remarkably high preference to reside around the hydroquinone ring in these molecular shuttles. This observation illustrates how a very small constitutional difference-hydroquinone versus resorcinol recognition sites-can lead to the overwhelming preference for one translational isomer over another in this particular range of [2]rotaxanes.
