Organoboron compounds,

B. M. Mikhailov and Yu. N. Bubnov, Organoboron Compounds in Organic Synthesis, Harwood Academic PubHshers, London, 1984. 

RTIX2 compounds, eg, dichlorophenyltaHium(III) [19628-33-2], can be obtained from the reaction of thaHic haHde or carboxylate with an organoboron compound (22) ... 

AbRfi (or AIR3) react readily with ligands to form adducts, LAIR3. They are stronger Lewis acids than are organoboron compounds, BR3, and can be considered as hard (or class a)... 

Palladium-catalyzed cross-coupling with organoboron compounds... 

Palladium-catalyzed carbon-carbon bond forming reactions like the Suzuki reac-tion as well as the Heck reaction and the Stille reaction, have in recent years gained increased importance in synthetic organic chemistry. In case of the Suzuki reaction, an organoboron compound—usually a boronic acid—is reacted with an aryl (or alkenyl, or alkynyl) halide in the presence of a palladium catalyst. 

The preparation and analytical results of semipolar organoboron compounds containing Cl or P were reported and the surface activity and fireproofing mechanism of these substances were described [283]. 

Much attention has recently been focused on organoboronic acids and their esters because of their practical usefulness for synthetic organic reactions including asymmetric synthesis, combinatorial synthesis, and polymer synthesis [1, 3, 7-9], molecular recognition such as host-guest compounds [10], and neutron capture therapy in treatment of malignant melanoma and brain tumor ]11]. New synthetic procedures reviewed in this article wiU serve to find further appHcations of organoboron compounds. 

Darmency V, Renaud P (2006) Tin-Free Radical Reactions Mediated by Organoboron Compounds. 263 71-106... 

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