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Cross-coupling reactions organoborons

Cross-coupling with organoboron compounds (the Suzuki-Miyaura reaction) is by far the most popular and versatile method of cross-coupling, and has been extensively reviewed.3-5... [Pg.308]

Miyaura, N. Suzuki, A. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds, Chem. Rev. 1995, 95, 2457-2483. [Pg.76]

The Suzuki Coupling, which is the palladium-catalysed cross coupling between organoboronic acid and halides. Recent catalyst and methods developments have broadened the possible applications enormously, so that the scope of the reaction partners is not restricted to aryls, but includes alkyls, alkenyls and alkynyls. Potassium trifluoroborates and organoboranes or boronate esters may be used in place of boronic acids. Some pseudohalides (for example triflates) may also be used as coupling partners. [Pg.226]

Suzuki, A. Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles. J. Organomet. [Pg.301]

A. R. Martin, Y. Yang, Palladium Catalyzed Cross-Coupling Reactions of Organoboronic Acids with Organic Electrophiles "Acta Chem. Scand. 1993, 47, 221-230. [Pg.256]

S. Suzuki, Cross-Coupling Reactions of Organoboron Compounds with Organic Halides, in Metal-catalyzed Cross-coupling Reactions (F. Diederich, P. J. Stang, Eds.), Wiley-VCH, Weinheim, 1998, 49-89. [Pg.733]

MiyauraN, Suzuki A (1995) Palladium-catalyzed cross-coupling reactions of organoboron compounds. Chem Rev 95 2457-2483... [Pg.32]


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See also in sourсe #XX -- [ Pg.461 , Pg.463 ]




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Cross-coupling reactions of organoboron compounds

Organoboron

Organoboron compounds cross-coupling reactions

Organoboron compounds metal-catalyzed cross-coupling reactions, with organic

Organoboronates

Organoborons

Palladium-catalyzed cross coupling reaction of organoboron compounds

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