1165-58-8Relevant articles and documents
Role of the base and control of selectivity in the suzuki-miyaura cross-coupling reaction
Lima, Carlos F. R. A. C.,Rodrigues, Ana S. M. C.,Silva, Vera L. M.,Silva, Artur M. S.,Santos, Luis M. N. B. F.
, p. 1291 - 1302 (2014)
The outcome of the Suzuki-Miyaura cross-coupling for the direct competition reaction between two boronic acids was evaluated under routine synthesis conditions. The reaction selectivity was found to depend on the amount of the base used, with fewer bases
Acid-catalyzed rearrangements in arenes: Interconversions in the quaterphenyl series
Skraba-Joiner, Sarah L.,Holt, Carter J.,Johnson, Richard P.
, p. 2655 - 2663 (2019/12/11)
Arenes undergo rearrangement of phenyl, alkyl, halogen and other groups through the intermediacy of ipso arenium ions in which a proton is attached at the same carbon as the migrating substituent. Interconversions among the six quaterphenyl isomers have b
Polyphenyl synthesis by means of the Kharash-type Grignard cross-coupling reaction
Ibuki,Ozasa,Fujioka,et al.
, p. 2369 - 2379 (2007/10/02)
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