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Gold catalysis transfer hydrogenation

Ferrocenylphosphine-gold complexes, 225 Formaldehyde oligomerization, 332 Formic acid, transfer hydrogenation, 123 Formulas, chiral compounds, xiii-xvii Four-dimensional chemistty. See Asymmetric catalysis... [Pg.194]

Scheme 7.67 Tandem hydroamination-hydroarylation-transfer hydrogenation reaction catalysed by gold catalysis and chiral phosphoric acid... Scheme 7.67 Tandem hydroamination-hydroarylation-transfer hydrogenation reaction catalysed by gold catalysis and chiral phosphoric acid...
Han Z-Y, Xiao H, Chen X-H, Gong L-Z. Consecutive intramolecular hydroamination/asymmetric transfer hydrogenation under relay catalysis of an achiral gold complex/chiral brpnsted acid binary system. J. Am. Chem. Soc. 2009 131 9182-9183. [Pg.1205]

Gold(in).—Several papers have appeared on the reactions of [AuClJ" with mono-and di-carboxylic acids. In general the reduction is preceded by a substitution reaction at the oxidant. Preliminary data indicate that the chloride-ion dependence of the rates of reduction of methyl and dimethyl malonates varies markedly between the two substrates. Confirmation of this aspect is provided in a later paper where the catalysis by Cl is attributed to an interaction of the chloride ion with a hydrogen on the central CHX moiety of the substituted malonic acid. Second-order rate constants increase in the manner k = k +k [C ] and a mechanism of reaction involves reaction of [AuCl and [AuCljCOH)]" with the free acid and the chloro adduct. In the rate-determining electron transfer [AuC ]-, Au , and COj are produced. [Pg.100]


See other pages where Gold catalysis transfer hydrogenation is mentioned: [Pg.277]    [Pg.280]    [Pg.277]    [Pg.280]    [Pg.131]    [Pg.951]    [Pg.951]    [Pg.59]    [Pg.151]    [Pg.179]    [Pg.55]    [Pg.60]    [Pg.935]    [Pg.144]    [Pg.402]    [Pg.229]   
See also in sourсe #XX -- [ Pg.156 ]




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