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Reductive group

This concept can be extended to mixtures if the pseudo-critical constants of the mixture and a mixture reduction group are defined. This gives the... [Pg.111]

T = pseudo-critical temperature of the mixture P = pseudo-critical pressure of the mixture Xr — reduction group for the property ij/, for example (/ for enthalpy... [Pg.111]

N. Chriss and V. Ginzburg, Representation theory and complex geometry (Geometric techniques in representation theory of reductive groups) , Progress in Math. Birkhauser, (to appear). [Pg.113]

Solvable groups play an important role in the further structural analysis of arbitrary algebraic groups. We can do little more here than mention a few of the major concepts (see also (12.5) on reductive groups). For simplicity we... [Pg.86]

Finally, reductive groups play a major role in recent work on automor-phic functions. To take the basic example, let k be the reals. Then SL2(k) acts on the half-plane 2 = x + iy y > 0 by ( J)z = (az + b)/(cz + d) this is transitive, and the circle group K - ( g ) a2 + b2 = 1 is the stabilizer of z = i. Thus the half-plane is the coset space (symmetric space) for K in SLz(k). The classical modular functions on the half-plane are precisely those invariant under the arithmetic subgroup SL2(Z) or certain subgroups of it. All such functions can thus be pulled back to be functions on SL2(k) with certain invariance properties. The same thing then can be done for coset spaces of other reductive groups. Some of the most recent treatments also use the group not just for the reals but for the various p-adic completions of... [Pg.55]

A particular example of reductive group elimination is elimination of a A-oxide function. Because of the rich chemistry of azine A-oxide it is often expedient to carry over useful functionalizations at the A-oxide level and then to reduce such a... [Pg.1033]

The reaction of an alkyl halide with lithium was cited earlier (Section 2.16) as an example of an oxidation-reduction. Group I metals are powerful reducing agents. [Pg.549]

Within the OECD, where the Pesticide Forum, and in particular the Risk Reduction Group, have expressed a need for reliable usage statistics. [Pg.12]

Fig. 8.4 Relative distributions of total ocean area and of global ocean oxygen uptake or sulfate reduction, grouped into five depth zones of the ocean. Based on data compiled hy Canfield (1993) and Canfield et al. (2005). Fig. 8.4 Relative distributions of total ocean area and of global ocean oxygen uptake or sulfate reduction, grouped into five depth zones of the ocean. Based on data compiled hy Canfield (1993) and Canfield et al. (2005).
Many enzymes are active in hydrolyses, and operate by acid-base catalysis. This is because the polypeptide chain can provide high concentrations of protons from readily available amino and carboxyl functional groups. However, many of the reactions which occur in metabolism involve chemical processes other than acid-base catalysis, which cannot be mediated by the side chains of amino acids. These include oxidation-reduction, group transfer, isomerization, and bond-breaking and bond-making reactions. Proteins consisting only of amino acid residues cannot catalyze these processes. [Pg.454]

Fig. 3.12 TEM of HPS-Pt after H2 reduction. Groups of single Pt nanoparticles are highlighted by circles. Reprinted with permission from Ref [89]. Copyright (2001) American Chemical Society. Fig. 3.12 TEM of HPS-Pt after H2 reduction. Groups of single Pt nanoparticles are highlighted by circles. Reprinted with permission from Ref [89]. Copyright (2001) American Chemical Society.
While it is quite likely that individuals and groups who support very liberal legalization policies also support harm-reduction groups, that does not lead to a conclusion that harm-reduction groups are attempting to legalize drugs. However, that seems to be the position expressed in the NDCS. [Pg.57]

The chlorite-iodide reaction is clearly the minimal oscillator of the subfamily of chlorite-iodide xidant oscillating reactions, and, since iodate and iodine appear to be produced in all of them, it can be considered to be the progenitor of a still larger family that includes the chlorite-iodate-reductant and cWorite-iodine-reductant groups listed in Table 4.1. Clearly, the chlorite-iodide reaction cannot be minimal for the entire family of chlorite-based oscillators since many of them contain no iodine species. It is not at all obvious that a minimal oscillator for the entire chlorite family exists. [Pg.80]

Reactive groups. Some compounds have components that are self-reactive and are composed of an oxidative group together with a reductive group. These are called redox compounds (hydrazine, hydroxylamine, hydroxylammonium nitrate), and are unstable. [Pg.165]


See other pages where Reductive group is mentioned: [Pg.111]    [Pg.127]    [Pg.133]    [Pg.442]    [Pg.149]    [Pg.313]    [Pg.258]    [Pg.108]    [Pg.108]    [Pg.55]    [Pg.207]    [Pg.1486]    [Pg.173]    [Pg.58]    [Pg.267]    [Pg.569]    [Pg.651]   
See also in sourсe #XX -- [ Pg.97 ]

See also in sourсe #XX -- [ Pg.97 ]




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2.6- dinitrotoluene, nitro group reduction

Amide cleavage induced by nitro group reduction

Amino group nitro reduction

Amino groups reductive methylation procedure

Amino groups reversible reductive alkylation

Ammonium sulfide nitro group reduction

Aromatic carbonyl groups, reduction

Aromatic nitro group, reduction

Benzyl group reduction

Benzyloxycarbonyl group, reductive cleavage

By Alan Cox 2 Reduction of the Carbonyl Group

Carbonyl group oxidation and reduction

Carbonyl group reduction

Carbonyl group selective reduction

Carbonyl group, reduction resonance structures

Carbonyl groups hydride reduction

Carbonyl groups stereoselective reductions

Carbonyl reduction Lewis basic functional groups

Carboxy groups enzymic reduction

Carboxyl groups reduction

Carboxyl groups, protection reduction

Carboxylic acids carboxyl groups reduction

Chemoselective carbonyl group reduction

Conjugate reduction group 14 metal hydrides

Cyano group, reduction

Diazo groups reductive removal

Electrocatalysis reduction, functional groups

Ester groups films, reduction

Functional Group Transformations Oxidation and reduction

Functional groups model protein reduction

Functional groups reductive conversions

Functional groups selective reduction

Group cleavage, reductive

Group reduction function

Group theory representation reduction

Group transfer reactions reduction

Hydride Reduction of a Carbonyl Group

Hydroxyl groups formation by reduction

Iron complexes acyl group reductions

Metal groups carbonylates, reductive elimination reactions

Metal groups palladium-catalyzed reductive coupling

Molecular weight reduction groups

Nitro group polarographic reduction

Nitro group reduction

Nitro groups, reduction aldehydes

Nitro groups, reduction amines

Nitro groups, reduction disulfides

Nitro groups, reduction esters

Nitro groups, reduction oximes

Nitro groups, reduction sulfonic acids

Nitro groups, substituted benzenes reduction

Nitrogen-containing compounds nitro group reduction

Nitrosyl group electrochemical reduction

Platinum group metals reduction

Pre-Reduction of Carbonyl Groups with Lithium Aluminum Hydride

Preferential reduction groups

Protecting Groups Cleaved by Dissolving Metal Reduction

Protecting Groups Cleaved by Reductive Elimination

Protecting groups reduction-labile

Protective groups reductive

Protective groups reductive, total

Reactions at the Carbonyl Group—Oxidation and Reduction

Reducible Functional Groups Reductive Amination with Carboxylic Acids

Reduction functional groups

Reduction group

Reduction group

Reduction group 13 molecules

Reduction of Carbonyl and Other Functional Groups

Reduction of Carboxyl Groups

Reduction of Functional Groups

Reduction of Main Group Oxides via Metal Carbonyls and Carbonylate Anions

Reduction of Nitro- to Amino-groups

Reduction of Other Functional Groups

Reduction of Other Functional Groups by Hydride Donors

Reduction of activated carbonyl groups

Reduction of aromatic nitro groups

Reduction of carbonyl groups

Reduction of keto group

Reduction of nitro groups

Reduction of sulfur groups

Reduction of the 3-oxo group

Reduction of the Diazo Group

Reduction of the Ester Groups

Reduction of the carbonyl group

Reduction reaction nitro groups

Reductions nitro groups, palladium®) acetate

Reductions of Heterocyclic N-Oxides and Aromatic Nitro Groups

Reductions with sodium borohydride without protecting groups

Reductive Deoxygenation of Carbonyl Groups

Reductive Deoxygenation of Carbonyl Groups to Methylene

Reductive Removal of Chalcogen Groups (RS and RSe)

Reductive Removal of Functional Groups

Reductive Removal of Mercapto-groups

Reductive desulfurization thiocarbonyl group

Reductive elimination leaving groups

Selective Reduction of Functional Groups

Selective reduction of carbonyl group in

Special Activity Group on Accident Reduction

Standard reduction potentials group 1 metals

Stereoselective reductions, of carbonyl groups

Steric effects, of silyl groups (eont on reduction

Sulfonyl group, reduction

The Role of Proximal, Lewis Basic Functional Groups in Carbonyl Reduction

Tin reduction of nitro groups

Trichloromethyl group reduction

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