50847-06-8Relevant academic research and scientific papers
CuOx/OMS-2 catalyzed synthesis of 4,5-dicyano-1H-imidazoles moiety: Directly access to D-A system for AIE-active mechanofluorochromic materials
Zheng, Kaibo,Chen, Hui,Xiao, Yufeng,Yan, Jiaying,Zhang, Nuonuo,Liu, Xiang
, (2021/11/16)
Although a lot of mechanofluorochromic (MFC) materials have been reported, it still needs to be further explored due to the lack of the universal design principle. The AIE moiety molecules with D-A framework have been widely regarded as the ideal structur
Discovery of cell-active phenyl-imidazole Pin1 inhibitors by structure-guided fragment evolution
Potter, Andrew,Oldfield, Victoria,Nunns, Claire,Fromont, Christophe,Ray, Stuart,Northfield, Christopher J.,Bryant, Christopher J.,Scrace, Simon F.,Robinson, David,Matossova, Natalia,Baker, Lisa,Dokurno, Pawel,Surgenor, Allan E.,Davis, Ben,Richardson, Christine M.,Murray, James B.,Moore, Jonathan D.
scheme or table, p. 6483 - 6488 (2010/12/18)
Pin1 is an emerging oncology target strongly implicated in Ras and ErbB2-mediated tumourigenesis. Pin1 isomerizes bonds linking phospho-serine/threonine moieties to proline enabling it to play a key role in proline-directed kinase signalling. Here we report a novel series of Pin1 inhibitors based on a phenyl imidazole acid core that contains sub-μM inhibitors. Compounds have been identified that block prostate cancer cell growth under conditions where Pin1 is essential.
Reactivity of diazoazoles and azolediazonium salts in C-azo coupling reactions
Sadchikova,Mokrushin
, p. 354 - 365 (2007/10/03)
The comparative reactivity of heterocyclic diazo compounds and the corresponding diazonium salts in C-azo coupling reactions was studied using imidazole, pyrazole, and triazole derivatives as examples.The reactivities of pyrazole- and imidazole-derived di
Reactivity of Diazoazoles with Electron-rich Double Bonds
Cabre, Marta,Farras, Jaume,Sanz, Javier Fernandez,Vilarrasa, Jaume
, p. 1943 - 1950 (2007/10/02)
The energies of several intermediates that could arise from the reaction of diazoazoles with alkenes have been estimated by means of the MNDO and AM1 SCF-MO methods as well as, in some cases, by means of ab initio methods, at the 3-21G level.All the nine
