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Diarylborinic acids, catalysts

Gouliaras C, Lee D, Chan L, Taylor MS (2011) Regioselective activation of glycosyl acceptors by a diarylborinic acid-derived catalyst. J Am Chem Soc 133 13926-13929... [Pg.98]

Arylboron compounds with electron-withdrawing aromatic groups such as triarylborons, diarylborinic acids, and arylboronic acids represent a new class of air-stable and water-tolerant Lewis acid or Bronsted acid catalysts in organic synthesis. In particular, arylboronic acids are showing to be powerful tools in the design of chiral boron catalysts. [Pg.108]

Diarylborinic acids and arylboronic acids bearing electron-withdrawing substituents are useful as air-stable Lewis acid catalysts for various organic transformations. In particular, the potential of 3,5-(CF3)2C6H3B(OH)2 as a Lewis acid catalyst has strikingly increased since Yamamoto and Ishihara s initial study [32b]. Continued exploratory research on the application of arylboron compounds as air-stable and reusable catalysts is expected to provide powerful and practical methods for various Bronsted-Lewis acid-catalyzed organic transformations. [Pg.407]


See other pages where Diarylborinic acids, catalysts is mentioned: [Pg.221]    [Pg.509]    [Pg.121]    [Pg.123]    [Pg.130]    [Pg.508]    [Pg.536]    [Pg.111]    [Pg.112]    [Pg.377]    [Pg.377]    [Pg.380]   
See also in sourсe #XX -- [ Pg.111 , Pg.112 ]




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Diarylborinic acid

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