Hydrides elimination

P Eliminations, as will be seen later in this chapter, are important in many catalytic processes involving organometallic complexes. 

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This group was developed to minimize the problem of nitrogen allylation during the deprotection step, because deprotection proceeds with /3-hydride elimination. The derivative is stable to TFA and 6 N HCl. ... 

When less bulky ancillary ligands are used /3-hydride elimination leads to the formation of Q-olefins. As a consequence iminopyridine complexes are typically much less active than the diimine catalysts and afford lower-molecular-weight PE.321-324 For example, MAO/(122) polymerizes ethylene to branched oligomers with Mn < 600, and 240 branches per 1,000 carbons.325 Complex (123), is highly active for ethylene polymerization (820gmmol 1 h bar ).326 As with the diimine systems, reduction in the steric bulk of the ligand substituents results in reduced activity and lower-molecular-weight products. 

Most of these reactions are promoted with an inorganic base such as KOH, NaOH, or K2C03 as an essential co-catalyst. For reaction without alkaline bases see Mizushima et al.137 Many of these complexes contain a chloride ligand, which is easily displaced by an alkoxide displacement/ /3-hydride elimination sequence in the presence of a base to remove HC1 formed (Scheme 25). In contrast, cationic LnM+ systems add the alcohol by formation of M—O bond, with the base... 

Aryl-alkenyl cross-coupling is straightforward. Simple alkylmagnesium reagents (Me, Et, CH2SiMe3, etc.) can be easily involved in Ni-catalyzed cross-coupling (27),139,140 while more complex alkyl halides—particularly branched ones prone to /3-hydride elimination—require Pd catalysts with bidentate phosphines, such as dppf, to achieve good selectivity (Section 9.6.3.4.7). 

The selectivity in the Heck reaction of allylic alcohol 111 is interesting, and the factors that lead to the observed preference for (3-hydride elimination toward nitrogen in this system are unclear, although a combination of steric effects and stereoelectronic factors (i.e., alignment of C-H and C-Pd bonds, nN a c H interactions) is likely involved. Examination of related examples from the literature (Scheme 4.20) reveals no clear trend. Rawal and Michoud examined substrate 115, which lacks the influence of both the amine and hydroxyl substituents and also seems to favor (3-hydride elimination within the six-membered ring over formation of the exocyclic olefin under standard Heck conditions [18a]. However, under... 

Triphenylphosphine was obtained from Nakarai Chemicals, Japan. When the reaction is carried out without additional triphenylphosphine, the yield of coupling product may drop to 60-70% and the product is accompanied by the by-products, phenyl vinyl sulfide and 4-viny 1-1 -cyclohexene, derived from 3-hydride elimination. 

The branched polymers produced by the Ni(II) and Pd(II) a-diimine catalysts shown in Fig. 3 set them apart from the common early transition metal systems. The Pd catalysts, for example, are able to afford hyperbranched polymer from a feedstock of pure ethylene, a monomer which, on its own, offers no predisposition toward branch formation. Polymer branches result from metal migration along the chain due to the facile nature of late metals to perform [3-hydride elimination and reinsertion reactions. This process is similar to the early mechanism proposed by Fink briefly mentioned above [18], and is discussed in more detail below. The chain walking mechanism obviously has dramatic effects on the microstructure, or topology, of the polymer. Since P-hydride elimination is less favored in the Ni(II) catalysts compared to the Pd(II) catalysts, the former system affords polymer with a low to moderate density of short-chain branches, mostly methyl groups. 

C-C bond formation can be favored over /3-hydride elimination by changing the nature of the catalyst. Hence, cyclizations can be mediated by iridium carbene complexes resulting from a formal intramolecular cross-coupling of the alkene with an. s -C-H bond (Equation (40)). 

The most fundamental reaction is the alkylation of benzene with ethene.38,38a-38c Arylation of inactivated alkenes with inactivated arenes proceeds with the aid of a binuclear Ir(m) catalyst, [Ir(/x-acac-0,0,C3)(acac-0,0)(acac-C3)]2, to afford anti-Markovnikov hydroarylation products (Equation (33)). The iridium-catalyzed reaction of benzene with ethene at 180 °G for 3 h gives ethylbenzene (TN = 455, TOF = 0.0421 s 1). The reaction of benzene with propene leads to the formation of /z-propylbenzene and isopropylbenzene in 61% and 39% selectivities (TN = 13, TOF = 0.0110s-1). The catalytic reaction of the dinuclear Ir complex is shown to proceed via the formation of a mononuclear bis-acac-0,0 phenyl-Ir(m) species.388 The interesting aspect is the lack of /3-hydride elimination from the aryliridium intermediates giving the olefinic products. The reaction of substituted arenes with olefins provides a mixture of regioisomers. For example, the reaction of toluene with ethene affords m- and />-isomers in 63% and 37% selectivity, respectively. 

Allyl methylcarbonate reacts with norbornene following a ruthenium-catalyzed carbonylative cyclization under carbon monoxide pressure to give cyclopentenone derivatives 12 (Scheme 4).32 Catalyst loading, amine and CO pressure have been optimized to give the cyclopentenone compound in 80% yield and a total control of the stereoselectivity (exo 100%). Aromatic or bidentate amines inhibit the reaction certainly by a too strong interaction with ruthenium. A plausible mechanism is proposed. Stereoselective CM-carboruthenation of norbornene with allyl-ruthenium complex 13 followed by carbon monoxide insertion generates an acylruthenium intermediate 15. Intramolecular carboruthenation and /3-hydride elimination of 16 afford the -olefin 17. Isomerization of the double bond under experimental conditions allows formation of the cyclopentenone derivative 12. 

The third transformation, by far the most encountered process, is the /3-hydride elimination which is the major and the fastest process in many cases (Scheme 49). The /3-elimination is usually followed by the reductive elimination to give the cycloadduct and regenerate the active metal species. Depending on the regioselectivity of the elimination (Ha or Hb), two dienes, 1,3- and/or 1,4-diene, can be obtained. The products of the latter case formally correspond to Alder-ene adducts (see Chapter 10.12). 

Based on a /rarcr-acetoxypalladation of the triple bond, Lu has developed a highly enantioselective (up to 87% ee) synthesis of 7-butyrolactones with Pd(n) catalysis (Scheme 73).280 Following the initial /ra/w-acetoxy-palladation, a plausible mechanism for this sequence involves an intramolecular carbopalladation of the pendant olefin, and deacetoxypalladation instead of the common /3-hydride elimination in the final step. 

The complexation of the two 7t-systems to Fe(0) species, followed by the oxidative cyclization, furnishes the iron(n) complex 408. After /3-hydride elimination, the reductive elimination affords the cycloadduct 406 (Scheme 101). 

Rhodium(i) complexes are excellent catalysts for the 1,4-addition of aryl- or 1-alkenylboron, -silicon, and -tin compounds to a,/3-unsaturated carbonyl compounds. In contrast, there are few reports on the palladium(n) complex-catalyzed 1,4-addition to enones126,126a for the easy formation of C-bound enolate, which will result in /3-hydride elimination product of Heck reaction. Previously, Cacchi et al. described the palladium(n)-catalyzed Michael addition of ArHgCl or SnAr4 to enones in acidic water.127 Recently, Miyaura and co-workers reported the 1,4-addition of arylboronic acids and boroxines to a,/3-unsaturated carbonyl compounds. A cationic palladium(n) complex [Pd(dppe)(PhCN)2](SbF6)2 was found to be an excellent catalyst for this reaction (dppe = l,2-bis(diphenyl-phosphine)ethane Scheme 42).128... 

Preparation of palladium enolates and their reactions (/3-hydride elimination to enones, migratory insertion to C-C multiple bonds, reductive coupling with allyl or aryl groups, etc.) have been reported. However, the nucleophilic addition of palladium enolates to C=0 and C=N bonds has been little investigated.463... 

Cyclization of 2-(l-alkynyl)XV-alkylidene anilines is catalyzed by palladium to give indoles (Equation (114)).471 Two mechanisms are proposed the regioselective insersion of an H-Pd-OAc species to the alkyne moiety (formation of a vinylpalladium species) followed by (i) carbopalladation of the imine moiety and /3-hydride elimination or (ii) oxidative addition to the imino C-H bond and reductive coupling. 

A mechanistic pathway is proposed based upon the observed regioselectivities and other results that were obtained during the exploration of the scope and limitations of the Alder-ene reaction.38 Initially, coordination of the alkene and alkyne to the ruthenium catalyst takes place (Scheme 5). Next, oxidative addition affords the metallocycles 42 and 43. It is postulated that /3-hydride elimination is slow and that the oxidative addition step is reversible. Thus, the product ratio is determined by the rate at which 42 and 43 undergo /3-hydride elimination. 

Insertion of the alkyne into the Pd-H bond is the first step in the proposed catalytic cycle (Scheme 8), followed by insertion of the alkene and /3-hydride elimination to yield either the 1,4-diene (Alder-ene) or 1,3-diene product. The results of a deuterium-labeling experiment performed by Trost et al.46 support this mechanism. 1H NMR studies revealed 13% deuterium incorporation in the place of Ha, presumably due to exchange of the acetylenic proton, and 32% deuterium incorporation in the place of Hb (Scheme 9). An alternative Pd(n)-Pd(iv) mechanism involving palladocycle 47 (Scheme 10) has been suggested for Alder-ene processes not involving a hydridopalladium species.47 While the palladium acetate and hydridopalladium acetate systems both lead to comparable products, support for the existence of a unique mechanism for each catalyst is derived from the observation that in some cases the efficacies of the catalysts differ dramatically.46... 

Gycloisomerization of a disubstituted alkyne sometimes required activation of the alkyne by the addition of a conjugated carbonyl and performing the reaction at a higher temperature as in Equation (38). The geometry of the alkene determines the regioselectivity of the /3-hydride elimination, as ( )-60 gave predominantly 61 (Equation (38)), while 62 was the major product of the cycloisomerization of (Z)-60 (Equation (39)). 

The [4+ 4]-homolog of the [4 + 2]-Alder-ene reaction (Equation (48)) is thermally forbidden. However, in the presence of iron(m) 2,4-pentanedioate (Fe(acac)3) and 2,2 -bipyridine (bipy) ligand, Takacs57 found that triene 77 cyclizes to form cyclopentane 78 (Equation (49)), constituting an unprecedented formal [4 + 4]-ene cycloisomerization. The proposed mechanism for this transformation involves oxidative cyclization followed by /3-hydride elimination and reductive elimination to yield the cyclized product (Scheme 18). 

The proposed catalytic cycle of the ruthenium-catalyzed intermolecular Alder-ene reaction is shown in Scheme 21 (cycle A) and proceeds via ruthenacyclopentane 100. Support for this mechanism is derived from the observation that the intermediate can be trapped intramolecularly by an alcohol or amine nucleophile to form the corresponding five-or six-membered heterocycle (Scheme 21, cycle B and Equation (66)).74,75 Four- and seven-membered rings cannot be formed via this methodology, presumably because the competing /3-hydride elimination is faster than interception of the transition state for these substrates, 101 and 102, only the formal Alder-ene product is observed (Equations (67) and (68)). 

Interestingly, experimental results indicate that pathway II might be operative in some ruthenium(n)-catalyzed [5 + 2]-reactions. Cyclized products implicating /3-hydride elimination and subsequent reductive elimination from ruthenacyclopentenes have been reported (Scheme 17).26 A direct comparison with rhodium catalysts using these specific substrates has not been reported. 

Disubstituted silole derivatives are synthesized by the palladium-catalyzed reaction of (trialkylstannyl)di-methylsilane with terminal alkynes (Equation (107)).266 The mechanism is supposed to involve a palladium silylene complex, which is generated via /3-hydride elimination from LJ3d(SiMe2H)(SnBu3) (Scheme 62). Successive incorporation of two alkyne molecules into the complex followed by reductive elimination gives rise to the silole products. 

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