54932-37-5Relevant academic research and scientific papers
Synthesis of tetraarylpyridines by chemo-selective Suzuki-Miyaura reactions of 3,5-dibromo-2,6-dichloropyridine
Reimann, Sebastian,Parpart, Silvio,Ehlers, Peter,Sharif, Muhammad,Spannenberg, Anke,Langer, Peter
, p. 6832 - 6838 (2015/06/25)
Chemoselective Suzuki-Miyaura reactions on 3,5-dibromo-2,6-dichloropyridine were studied. The optimized reaction conditions allow for the facile access of 3-aryl- and 3,5-diarylpyridines in good yields. Suzuki-Miyaura reactions of the selectively synthesi
Site-selective synthesis of arylated pyridines by Suzuki-Miyaura reactions of 2,3,5,6-tetrachloropyridine
Reimann, Sebastian,Ehlers, Peter,Parpart, Silvio,Surkus, Annette,Spannenberg, Anke,Langer, Peter
supporting information, p. 5371 - 5384 (2015/07/15)
Site-selective arylation of commercially available 2,3,5,6-tetrachloropyridine has been accomplished, using the Suzuki-Miyaura reaction. The reaction conditions were thoroughly optimized, allowing the selective synthesis of mono-, di-, tri- and tetraarylated pyridines in good to quantitative yields. In addition, we studied the electrochemical properties of selected tetraarylpyridines by DPV-measurements.
