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Alkylmetal

Nitromethane Acids, alkylmetal halides, hydroxides, hydrocarbons, organic amines, formaldehyde, nitric acid, perchlorates... [Pg.1210]

Belonging to group (i) are alkylmetal carbonyls and cyclopentadienylmetal alkyl carbonyls of formula RMn(CO)5, CpFe(CO)2R, and CpMo(CO)3R. Solvent dependence of the reaction of MeMn(CO)5 with CjHi,NH2 is illustrated also in Table I. The rate varies markedly with the dielectric constant and with the nucleophilic power of the solvent. For example, on going from dimethylformamide to mesitylene, the rate of insertion is reduced by 10. Similarly, the sequence MeCN > MejCO > THF > CHCI3 > CjHj was reported for the reaction of MeMn(CO)5 with P(0CH2)3CR (R = Me and Et) in various solvents (97). Analogous trends were observed for the insertion reactions of CpFe(CO)2R and CpMo(CO)3R (48, 80, 98). [Pg.97]

The catalytic enantioselective addition of vinylmetals to activated alkenes is a potentially versatile but undeveloped class of transformations. Compared to processes with arylmetals and, particularly alkylmetals, processes with the corresponding vinylic reagents are of higher synthetic utility but remain scarce, and the relatively few reported examples are Rh-catalysed conjugate additions. In this context, Hoveyda et al. reported very recently an efficient method for catalytic asymmetric allylic alkylations with vinylaluminum reagents that were prepared and used in Thus, stereoselective reactions... [Pg.52]

See Nitromethane Alkylmetal halides See Other ALKYLALUMINIUM HALIDES... [Pg.173]

See Sodium acv-nitromethanide, 2-Nitroacetaldehyde oxime Alkylmetal halides... [Pg.184]

Alkylstibines decompose explosively on heating or shock. See other alkylmetal hydrides... [Pg.201]

See Other AGITATION INCIDENTS, ALKYLMETAL HALIDES, GRIGNARD REAGENTS... [Pg.327]

See other alkylmetals, endothermic compounds, mercury compounds... [Pg.339]

Propyllithium [2417-93-8] PrLi Leleu, Cahiers, 1977, (88), 368 It ignites in air. See other alkylmetals C3H7Li... [Pg.446]

See METAL DERIVATIVES OF ORGANOFLUORINE COMPOUNDS See entry TRIALKYLALUMINIUMS See Other ALKYLMETALS... [Pg.458]


See other pages where Alkylmetal is mentioned: [Pg.78]    [Pg.84]    [Pg.228]    [Pg.161]    [Pg.162]    [Pg.173]    [Pg.174]    [Pg.178]    [Pg.180]    [Pg.180]    [Pg.180]    [Pg.180]    [Pg.181]    [Pg.190]    [Pg.232]    [Pg.287]    [Pg.302]    [Pg.303]    [Pg.328]    [Pg.332]    [Pg.333]    [Pg.335]    [Pg.335]    [Pg.335]    [Pg.336]    [Pg.336]    [Pg.337]    [Pg.339]    [Pg.339]    [Pg.353]    [Pg.353]    [Pg.424]    [Pg.446]    [Pg.451]    [Pg.460]    [Pg.462]    [Pg.462]    [Pg.466]    [Pg.466]    [Pg.468]   


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ALKYLMETAL HALIDES

ALKYLMETAL HYDRIDES

Alkyl halides alkylmetal coupling

Alkylmetal bonds

Alkylmetal complexes, formation

Alkylmetal donors

Alkylmetal donors ionization potentials

Alkylmetal insertion

Alkylmetal reagents

Alkylmetal-hydride complexes

Alkylmetals

Alkylmetals alkylation

Alkylmetals electron transfer

Alkylmetals ionization

Alkylmetals reactivity

Alkylmetals, alkyl groups

Aniline, o-alkylmetal complexes

Aniline, o-alkylmetal complexes addition reactions

Aryl halides, cross coupling with alkylmetals

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

Electron alkylmetals

Initiation by alkylmetals

Isomerization, Rearrangement, and Redistribution of Alkylmetal Compounds

Organometallic alkylmetals

Palladium-Catalyzed Cross-Coupling nvolving Saturated Alkylmetals

Redox alkylmetals

Transition metal catalyst active in absence of alkylmetals

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