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Lodination, of thiophene

Boron Reagents. lodination of 3,4-bis(trimethylsilyl)thiophene followed by a Suzuki phenylation gives the monophenylated product 3-phenyl-4-trimethylsilylthiophene 45 (Scheme 23). After another ipso-iodination using iodine and silver trifluoroactetate and Suzuki coupling at the iodo carbon, 3,4-diarylated thiophenes are produced.The same reactions have been effected in furans. ... [Pg.425]

See other pages where Lodination, of thiophene is mentioned: [Pg.820]    [Pg.57]    [Pg.1017]    [Pg.254]    [Pg.55]    [Pg.123]    [Pg.820]    [Pg.57]    [Pg.1017]    [Pg.254]    [Pg.55]    [Pg.123]    [Pg.200]    [Pg.51]    [Pg.123]    [Pg.195]    [Pg.73]   
See also in sourсe #XX -- [ Pg.30 , Pg.53 ]



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Lodination

Of thiophene

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