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One reduction

The catalyst is also employed in the form of the finely-divided metal deposited upon activated carbon (usually containing 5 or 10 per cent. Pd) two methods of preparation are described, in one reduction is effected with alkaline formaldehyde solution and in the other with hydrogen ... [Pg.949]

H-Dibenz[6,dJazepin-6-one, 6,7-dihydro-alkylation, 7, 518 Dibenz[6,dJazepin-7-one reduction, 7, 525... [Pg.599]

Enantioselective 1,4-reduction of enones can be done using a copper-BINAP catalyst in conjunction with silicon hydride donors.158 Polymethylhydrosilane (PMHS) is one reductants that is used. [Pg.419]

Another classic reaction of pyridinium salts is reduction of the pyridine ring. Donohoe and co-workers reported the partial reduction of A-alkylpyridinium salts <060BC1071>, which is accompanied by subsequent alkylation and hydrolysis to furnish a range of 2,3-dihydropyrid-4-ones. This sequence has the potential to introduce a variety of functional groups at the C-2 position of 2,3-dihydropyrid-4-ones. Reduction of pyridinium ylides with sodium borohydride has also been reported in fair to good yields <06JHC709>. [Pg.323]

For mixed lanthanide-transition metal clusters, Yukawa et al. have synthesized an octahedral [SmNi6] cluster by the reaction of Sm3+ and [Ni(pro)2] in nonaque-ous medium [66-68]. The six [Ni(pro)2] ligands use 12 carboxylate oxygen atoms to coordinate to the Sm3+ ion, which is located at the center of an octahedral cage formed by six nickel atoms. The coordination polyhedron of the central Sm3+ ion may be best described as an icosahedron. The [SmNir, core is stable in solution but the crystal is unstable in air. The cyclic voltammogram shows one reduction step from Sm3+ to Sm2+ and six oxidation steps due to the Ni2+ ions. Later, similar [LaNis] and CjdNif> clusters were also prepared. [Pg.174]

A From Table 21-1 we choose one oxidations and one reductions reaction so as to get the least negative cell voltage. This will be the most likely pair of Vi -reactions to occur. [Pg.511]

The repeated treatment with lithium aluminum hydride was necessary to obtain complete reduction, since use of the reducing agent in manyfold excess and longer reaction times failed to accomplish complete reduction in one step. If the product was purified by distillation without the second reduction, the yield of pure diimine amounted to 9.1 g. (71%). The submitters report that on ten times the scale the yield with one reduction was 81 g. (64%). [Pg.116]

The same current will be passed through the working and counter electrodes (albeit, one oxidative and one reductive). By inserting the relevant values into equation (1.1), we obtain a value of i = 0.06 A cm , so therefore the maximum value of i is not reached. [Pg.321]

An electrochemical model for the process of electroless metal deposition was suggested by Paunovic (10) and Saito (8) on the basis of the Wagner-Traud (1) mixed-potential theory of corrosion processes. According to the mixed-potential theory of electroless deposition, the overall reaction given by Eq. (8.2) can be decomposed into one reduction reaction, the cathodic partial reaction. [Pg.140]

In uremia there are present in the serum a variety of known and unknown metabolites that can produce aberrant laboratory results. Significant differences in glucose concentration have been observed in such specimens analyzed by ferricyanide (F2a) or Fe (II)-5-pyridylbenzo-diazepin-2-one reduction methods compared to glucose oxidase procedures (K7a). In a patient with elevated creatinine (15 mg/100 ml) and uric acid (10 mg/100 ml), the glucose value determined by the automated alkaline ferricyanide procedure was overestimated by 20 mg/100 ml (C4). In uremic patients undergoing chronic hemodialysis there is a decrease in transaminase activity. In 11 of 19 such patients, there was... [Pg.28]

In the voltammogram of Au(lll) modified with binary SAM of 1-undecanethiol and 11-mercaptoundecanoic acid, only one reductive desorption peak was formed for any value of mixing ratio of both thiols [139]. Such a response suggests that both thiols are well mixed in the SAM. [Pg.859]

Redox reactions always consist of one oxidation reaction and one reduction reaction. The separate oxidation and reduction reactions are known as half reactions. The sum of the two half reactions gives the overall reaction. When the half reactions are summed, there is an equal number of elec-... [Pg.177]

It is important to recognise that some or any of these symptoms can be very severe, particularly if the withdrawal is too rapid and the person has not stabilised following one reduction when another... [Pg.109]

Reductions were carried out in the electrolysis vessel shown in Figure 1. One reduction (No. 14) was carried out in a divided cell provided with a... [Pg.512]


See other pages where One reduction is mentioned: [Pg.283]    [Pg.735]    [Pg.882]    [Pg.119]    [Pg.401]    [Pg.1506]    [Pg.262]    [Pg.531]    [Pg.257]    [Pg.87]    [Pg.544]    [Pg.96]    [Pg.172]    [Pg.217]    [Pg.97]    [Pg.695]    [Pg.57]    [Pg.158]    [Pg.1158]    [Pg.654]    [Pg.704]    [Pg.843]    [Pg.279]    [Pg.735]    [Pg.882]    [Pg.2093]   
See also in sourсe #XX -- [ Pg.186 ]

See also in sourсe #XX -- [ Pg.98 ]




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1- -ethanone one-electron reduction potential

1.2.4- Triazol-5-ones reduction

1.6.7.8- Tetrahydro-4//-pyrido pyrimidin-4-ones, reduction

2- Oxazolin-5-ones reduction

2- Pyrazolin-5-ones reduction

2-Amino-3-nitroso-4//-pyrido pyrimidin-4-ones, reduction

4- Nitropyrazol-3-ones, reduction

4//-Pyrido pyrimidin-4-ones reduction

9 perhydropyrido oxazin-1-ones, reduction

And one-electron reduction potential

C-Glycosyl compounds one-electron reduction

Cholest-4-en-3-one reduction

Cholest-4-en-3-one reductive elimination

Concerted one-electron reductions

Consecutive and Cascade One-Pot Reductions

Imidazolidin-2-ones reduction

One electron oxidation and reduction

One-Electron Reduction and Oxidation in Nonaqueous Solvents

One-Electron Reductions of Carbonyl Compounds and Esters Reductive Coupling

One-electron enzymatic reduction

One-electron oxidation/reduction

One-electron reductants

One-electron reduction

One-electron reduction pathway

One-electron reduction potential

One-electron reduction process

One-electron reduction product

Oxadiazin-5-ones reduction

Pyridazin-3-ones, reduction

Pyrimidin-2 -ones reduction

Reduction of Heterocycles Containing One Nitrogen Atom

Reduction of a System on One Isolated Level Surface

Reduction of azetidin-2-ones (3-lactams)

Reduction of cholest-5-en-3-one

Reduction to a One-Parameter Model

Reductions of Other Heterocycles Containing One Nitrogen Atom

Reversible one-electron reduction and

Tetrahydro-1,3-oxazin-2-ones, reduction

Triazine-3-ones, reduction

Two- step one-electron reduction

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