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Silver terphenyl

Methods D and E are very efficient non-aqueous, rather neutral procedures applying silver(I) and thallium(I) carbonates, but useful only for small-scale labo-synthesis started from boronic esters [17-19]. An illustrative example is the reaction of 1,4-bispinacolboronic ester 266 with iodobenzene affording / -terphenyl (267) in essentially quantitative yield [18], respectively. Scheme 15. [Pg.156]

Silver carbonate as the base in the SM reaction with arylboronic ester Preparation ofp-terphenyl (267) /ISf... [Pg.193]

See other pages where Silver terphenyl is mentioned: [Pg.88]    [Pg.941]    [Pg.17]    [Pg.23]    [Pg.926]    [Pg.292]    [Pg.131]    [Pg.45]    [Pg.335]    [Pg.193]    [Pg.6235]    [Pg.3738]    [Pg.105]    [Pg.106]    [Pg.193]    [Pg.215]   
See also in sourсe #XX -- [ Pg.105 ]



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