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Phenylpyridine cores

Switching from the biphenyl core to a 3-phenylpyridine core resulted in compounds that were similar in potency to the biphenyl compounds, but with increased inhibition of ACC2 versus ACC1, as... [Pg.102]

In a similar way the pinene-phenylpyridine H[46] was prepared. Thus upon treatment of 4,5-(/f,/f)-pinene-2-phenylpyridine H[46] with IrCls.SHaO, the HEXOL-type tetranuclear iridium complexes [Ir IrCl2(46)2 3] were obtained as two isomers (5.67ab) in a ratio of 5 3 (Scheme 5.25). Each complex can be described as an inner core of HEXOL-type [Ir(IrCl2)3] units and a surface of six chiral bidentate cyclometallated ligands (46). [Pg.155]


See other pages where Phenylpyridine cores is mentioned: [Pg.95]    [Pg.102]    [Pg.95]    [Pg.102]    [Pg.227]    [Pg.617]    [Pg.422]    [Pg.191]    [Pg.241]    [Pg.287]    [Pg.1022]   
See also in sourсe #XX -- [ Pg.102 ]




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2-Phenylpyridine

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