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Alkyl cross-coupling

Cardenas, D. J. Towards efficient and wide-scope metal-catalyzed alkyl—alkyl cross-coupling reactions. Angew. Chem. Int. Ed. 1999,... [Pg.304]

Alkyl halides other than aryl and vinyl halides do not readily undergo oxidative addition with Pd and must, in general, first be converted to alkylmetals. In this connection, however, a recent report on the Ni catalysed selective alkyl-alkyl cross-coupling with Ni(acac)2 and Lil in THF represents a significant breakthrough.34 In cases where the alkyl group contains a p-H atom, reduction of the organic halide via p-dehydropalladation reductive elimination can be a serious side-reaction (Scheme 11.6). [Pg.222]

Fig. 12. Two-electron mechanisms proposed by TAMREAC for the allyl-alkyl cross-coupling. The two numbers below each complex correspond to the complex number and to the valence electron number, respectively. Numbers in parentheses by the arrows correspond to the reaction numbers (Tables II, III, and IV). R = alkyl, X = halide, L = solvent molecule. Fig. 12. Two-electron mechanisms proposed by TAMREAC for the allyl-alkyl cross-coupling. The two numbers below each complex correspond to the complex number and to the valence electron number, respectively. Numbers in parentheses by the arrows correspond to the reaction numbers (Tables II, III, and IV). R = alkyl, X = halide, L = solvent molecule.
Fig. 13. One-electron nonchain mechanisms proposed by TAMREAC for the allyl—alkyl cross-coupling. Fig. 13. One-electron nonchain mechanisms proposed by TAMREAC for the allyl—alkyl cross-coupling.
Fig. 40 Alkyl-alkyl cross-coupling reactions catalyzed by Pd(0) complexes... Fig. 40 Alkyl-alkyl cross-coupling reactions catalyzed by Pd(0) complexes...
It has also been found that nickel-terpyridyl catalytic systems enable alkyl-alkyl cross-coupling with alkylzinc halides only using THF as solvent (Scheme 4.98) [299]. For instance, nPentZnBr undergoes coupling at rt and in excellent yields with 3-phenylpropyl iodide 425 in the presence of Ni(COD)2 (5 mol%) and tBu-Terpy (277) (5mol%). These catalytic systems have been studied in detail from... [Pg.338]

Alkyl-alkyl cross-coupling reactions have historically been the most difficult to realize. Among the many obstacles to the effective development of such a system are the lower reactivity of alkyl groups relative to alkenyl and aryl groups, as well as side processes such as -hydride elimination that are accessible with alkyl substrates. More reports by Fu et al. have disclosed successful alkyl cross-coupling protocols... [Pg.505]

A series of arylynamides with alkyloxy groups at the ortho position of the aryl group has been prepared by an alkylation/cross-coupling/amidation sequence and a subsequent gold-catalysed reaction provides benzofurans with amine functionalities at the 2-position and alkyl groups at the 3-position. The mechanism of gold(III)-catalysed isomerization of alkyl-substituted allenes to conjugated dienes in the presence of a... [Pg.566]

Scheme 2-31. Alkyl-alkyl cross-coupling reaction catalyzed by Cu(l)-salts. Scheme 2-31. Alkyl-alkyl cross-coupling reaction catalyzed by Cu(l)-salts.
Of-Silylalkanenitriles couples with aryl halides to give a variety of cx-arylalkanenitriles (Scheme 3-169). On the other hand, alkyl cross-coupling reaction using alkylsilane reagents as nucleophiles is successful only with... [Pg.481]

Ishiyama T, Abe S, Miyaura N, Suzuki A. Palladium-catalyzed alkyl-alkyl cross-coupling reaction of 9-Alkyl-9-BBN derivatives with iodoalkanes possessing (i-hydrogens. Chem. Lett. 1992 21(4) 691-694. [Pg.393]


See other pages where Alkyl cross-coupling is mentioned: [Pg.315]    [Pg.411]    [Pg.100]    [Pg.166]    [Pg.202]    [Pg.328]    [Pg.370]    [Pg.1298]    [Pg.31]    [Pg.600]    [Pg.163]    [Pg.88]    [Pg.119]    [Pg.219]    [Pg.241]    [Pg.799]    [Pg.42]    [Pg.193]   
See also in sourсe #XX -- [ Pg.483 ]




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Alkenyl-aryl cross-coupling alkylation

Alkyl Hiyama cross-coupling

Alkyl Negishi cross-coupling

Alkyl Sonogashira cross-coupling

Alkyl Stille cross-coupling

Alkyl Suzuki cross-coupling

Alkyl bromides cross-coupling reactions

Alkyl bromides, Negishi cross-coupling

Alkyl bromides, Negishi cross-coupling reactions

Alkyl coupling

Alkyl cross coupling with copper

Alkyl cross-coupling reaction

Alkyl electrophiles, cross-coupling with

Alkyl esters, cross-coupling

Alkyl halides Kumada cross-coupling reactions

Alkyl iodides cross-coupling with Grignard reagents

Alkyl metals, vinyl halide cross-coupling

Alkyl tosylates, Suzuki cross-coupling

Alkylation cross-coupling

B-alkyl Suzuki-Miyaura cross-coupling

B-alkyl Suzuki-Miyaura cross-coupling reaction

Catalytic asymmetric cross-coupling reactions with secondary alkyl halides

Couplings alkylative

Cross-coupling Reactions of Alkyl Electrophiles

Cross-coupling alkyl bromides

Cross-coupling alkyl-alkenyl

Cross-coupling reactions alkyl electrophiles

Cross-coupling reactions alkyl halides

Cross-coupling reactions alkyl halides with Grignard reagents

Cross-coupling reactions alkylation

Cross-coupling reactions allylic alkylation

Cross-coupling reactions primary alkyl

Cross-coupling reactions secondary alkyl

Cross-coupling reactions tertiary alkyl

Cross-coupling reactions with alkyl halides

Ei-ichi Negishi and Baiqiao Liao 11 Palladium-Catalyzed Cross-Coupling Involving Alkylmetals or Alkyl Electrophiles

Kumada cross-coupling reactions, palladium alkyl halides

Negishi cross-coupling, alkyl electrophile

Organozinc reagents cross-coupling reactions with alkyl halides

PALLADIUM CATALYSED CROSS-COUPLING REACTIONS 2 Allylic alkylation

Palladium-catalyzed cross-coupling involving alkyl groups without proximal unsaturation

Stille cross-coupling, alkyl electrophile

Suzuki cross-coupling alkyl halides

Suzuki cross-coupling, alkyl electrophile

Zinc reagents cross-coupling with alkyl halides

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