910036-88-3Relevant academic research and scientific papers
Discovery of thienothiazolocarboxamide analogues as novel anti-tubercular agent
Carla, Virginia,Choi, Inhee,Choi, Junghwan,Delorme, Vincent,Heo, Jinyeong,Jea Seo, Jeong,Jin, Guanghai,Kang, Juhee,Kang, Sunhee,Kim, Jaeseung,Lee, Aram,Lee, Honggun,Lee, Sumi,Mi Kim, Young,Park, Kaapjoo,Park, Sinyoung,Seo, Mooyoung,Shum, David,Woo, Minjeong
, (2020)
In order to identify anti-tubercular agents with a novel scaffold, commercial libraries of small organic compounds were screened against a fluorescent strain of Mycobacterium tuberculosis H37Rv, using a dual phenotypic assay. Compounds were assessed again
Synthesis of functionalized 2-arylpyridines from 2-halopyridines and various aryl halides via a nickel catalysis
Gosmini, Corinne,Bassene-Ernst, Carine,Durandetti, Muriel
experimental part, p. 6141 - 6146 (2011/03/19)
An efficient nickel-catalyzed method devoted to the direct formation of functionalized 2-arylpyridines is described avoiding the prior preparation of organometallic species. Various functionalized 2-arylpyridines are obtained in moderate to excellent yields by a one-step chemical procedure from corresponding halides. The NiBr2(2,2′-bipyridine) complex appears to be an extremely suitable catalyst for the activation in the presence of manganese dust of aromatic halides and pyridyl halides functionalized by reactive groups. The versatility of this original process represents a simple alternative to most known methods using organometallic reagents.
