Cross coupling reactions involving radicals

Lithium intercalates are important in solid-state chemistry, and can be formed in heterogeneous reactions such as equation (46) [(M = Ti, Zr, Hf, V, Nb, Ta X = S, Se, Te R= n-Bu, s-Bu, t-Bu, n-Pr, CH2C(Me2)Ph]. Studies on product ratios of R to R2, cross-coupling reactions involving different R, and the influence of change of solvent, and comparisons with other systems, indicate the production of radicals, R, in a process which... 

In contrast to the transition metals, where there is often a change in oxidation level at the metal during the reaction, there is usually no change in oxidation level for boron, silicon, and tin compounds. The synthetically important reactions of these three groups of compounds involve transfer of a carbon substituent with one (radical equivalent) or two (carbanion equivalent) electrons to a reactive carbon center. Here we focus on the nonradical reactions and deal with radical reactions in Chapter 10. We have already introduced one important aspect of boron and tin chemistry in the transmetallation reactions involved in Pd-catalyzed cross-coupling reactions, discussed... 

Inhibition by radical traps, such as TEMPO 17, was used to explain the involvement of radicals in the course of transition metal-catalyzed reactions (Fig. 7). Typical cross-coupling reactions, such as Heck or Suzuki-Miyaura reactions, proceeded even with nitroxyls as substrates, although the yields were sometimes low. Thus, nitroxyls do not necessarily interfere very much with the course of two-electron catalytic processes [79-81]. However, it must be critically mentioned that 17 and related nitroxides are both oxidants and reductants for metal species. 

The most prominent reactions catalyzed by low-valent iron species involving radical intermediates are cross-coupling reactions of alkyl halides (recent reviews [32-35]) and atom transfer radical reactions. In cross-coupling reactions the oxidation state of the catalytically active species can vary significantly depending on the reaction conditions very often it is not known exactly. To facilitate a summary, all iron-catalyzed cross-coupling reactions are treated together and involved oxidation states, where known, are mentioned at the example. In contrast, iron-catalyzed Kharasch reactions will be treated at the oxidation state of the iron precursors. 

The purposes of this paper are then (a) to refer on some additional results obtained, in order to confirm the previously suggested [9, 10 ] involvement of humic free radicals in the cross coupling reactions of humic substances with xenobiotic phenoxy radicals and (b) to discuss comparatively the different behaviours of humic acids in these reactions, as a function of their different origin and chemical properties. 

An indium-mediated radical cyclization sequence has been used to synthesize stereoselectively 3-alkylideneoxindoles [65, 66]. The generation of predominantly the i -isomer, such as seen with 96 below, is attributed to the strong coordination of the indium to the carbonyl of the oxindole intermediate, and the transformation of various iodo-ynamides to the cyclized oxindoles occurred in good yield. Selective approaches to the E- and disubstituted 3-alkylideneoxindoles involving a tandem palladium-catalyzed cross coupling reaction were also highlighted in this report. 

It should be noted that addition of Lewis acidic salts, such as MgBt2, is critical in order to achieve an effective catalytic transformation when using arylzinc compounds. This observation indicates that the difficult step of the catalytic cycle is the transmetaUation of the aryl group from the zinc reagent to the catalytically active iron complex [42]. While the involvement of an intermediate radical species or a single electron-transfer process is suspected, mechanistic details of these iron-catalyzed cross-coupling reactions remain unclear. 

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