467252-18-2Relevant academic research and scientific papers
Indirect ortho functionalization of substituted toluenes through ortho olefination of N,N-dimethylbenzylamines tuned by the acidity of reaction conditions
Cai, Guixin,Fu, Ye,Li, Yizhou,Wan, Xiaobing,Shi, Zhangjie
, p. 7666 - 7673 (2008/02/09)
Highly regioselective olefination of substituted N,N-dimethylbenzylamines was developed by tuning the acidity of reaction conditions based on analysis of their features. The ortho-functionalized N,N-dimethylbenzylamines were further transformed into 3-(2′
Novel structures derived from 2-[[(2-pyridyl)methyl]thio]-1H-benzimidazole as anti-Helicobacter pylori agents, Part 1
Kühler, Thomas C.,Swanson, Marianne,Christenson, Beritte,Klintenberg, Ann-Charlotte,Lamm, Bo,F?gerhag, Jonas,Gatti, Roberto,?lweg?rd-Halvarsson, Maria,Shcherbuchin, Vladimir,Elebring, Thomas,Sj?str?m, Jan-Erik
, p. 4282 - 4299 (2007/10/03)
2-[[(2-Pyridyl)methyl]thio]-1H-benzimidazoles (2, sulfides) exhibit antibacterial properties that are selective for Helicobacter spp., but they also have an inherent susceptibility to metabolic oxidation to furnish 2-[[(2-pyridyl)methyl]sulfinyl]-1H-benzi
