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Substrates, hydrogenated

To illustrate how this applies in the present circumstances we consider a passible group transfer reaction between A2 dihydro-naphthalene, (gQ) > a hydrogen donor, and phenanthrene,(g gr > a substrate (hydrogen acceptor) which models a polynuclear aromatic moiety commonly found in coal. In the overall group transfer reaction ... [Pg.323]

In contrast to the high enantioselectivity achieved for the Z-isomeric substrates, hydrogenation of the S-isomeric substrates usually proceeds at a much lower rate and gives poor enantioselectivities [86]. With the Rh-BINAP system as the catalyst and tetrahydrofuran (THF) as solvent, hydrogenation of the Z-and S-isomeric substrates generates products with different configurations [2]. [Pg.865]

Entry Substrate Hydrogen donor Product Initial TOP ... [Pg.121]

Catalases bind or react with a number of molecules that can be either substrates (hydrogen peroxide and some small alcohols) or inhibitors (cyanide, azide, etc.) (see Section IV,B). Several such intermediates have... [Pg.92]

The detailed mechanism of P aeruginosa CCP has been studied by a combination of stopped-flow spectroscopy (64, 65, 84, 85) and paramagnetic spectroscopies (51, 74). These data have been combined by Foote and colleagues (62) to yield a quantitative scheme that describes the activation process and reaction cycle. A version of this scheme, which involves four spectroscopically distinct intermediates, is shown in Fig. 10. In this scheme the resting oxidized enzyme (structure in Section III,B) reacts with 1 equiv of an electron donor (Cu(I) azurin) to yield the active mixed-valence (half-reduced) state. The active MV form reacts productively with substrate, hydrogen peroxide, to yield compound I. Compound I reacts sequentially with two further equivalents of Cu(I) azurin to complete the reduction of peroxide (compound II) before returning the enzyme to the MV state. A further state, compound 0, that has not been shown experimentally but would precede compound I formation is proposed in order to facilitate comparison with other peroxidases. [Pg.197]

Two general cases have been encountered in which there appears to be almost complete suppression of solute-substrate hydrogen bonds even in monolayers, by reason of the groups in either solute or substrate being too strongly solvated by water. These are as follows ... [Pg.459]

The nitrosyl complex [Rh(NO)(PPh3)3] (36) catalyzes the hydrogenation of both 1-hexene and cyclohexene in dichloromethane as solvent and was also found to add deuterium to cyclohexene without H/D scrambling.138 A further study extended the range of substrates hydrogenated to internal alkenes, to conjugated and non-conjugated dienes, activated alkenes and terminal and internal alkynes.139... [Pg.244]

In contrast to the high enantioselectivities obtained for the Z substrates, hydrogenation of the E isomers usually proceeds very slowly and in a poor optical yield partly due to the E/Z double-bond isomerization. The enantioselectivity in the BINAP-Rh-catalyzed hydrogenation of E enamides is enhanced in an aprotic solvent THF to minimize the isomerization [15,56],... [Pg.11]

Substrate Hydrogen Source Catalyst % Yield % ee Confign... [Pg.77]

The activity and enantioselectivity of chiral Ir catalysts have been tested by using 2,3,3-trimethylindolenine as a model substrate. Hydrogenation of the cyclic imine with [Ir(bdpp)Hl2 2 gives the corresponding chiral amine with 80% ce (Scheme 1.99) [350]. The stereoselectivity is somewhat better than that with acyclic substrates (see Scheme 1.94). A neutral BCPM-Ir complex with Bil3 effects asymmetric hydrogenation in 91% optical yield [354], A complex of MCCPM shows similar enantioselection [354], These complexes are not applicable to the reaction of other acyclic and six-membered cyclic imines. An MOD-DIOP-Ir complex is also usable with the aid of ( -C4H9)4NI [355], An Ir complex of BICP with phthalimide effectively... [Pg.86]

Soedjak HS, Walker JV, Butler A (1995) Inhibition and Inactivation of Vanadium Bromoperoxidase by the Substrate Hydrogen Peroxide and Further Mechanistic Studies. Biochemistry 34 12689... [Pg.486]

Insofar as the substrate hydrogen is concerned, because of the high... [Pg.202]


See other pages where Substrates, hydrogenated is mentioned: [Pg.527]    [Pg.347]    [Pg.79]    [Pg.193]    [Pg.147]    [Pg.96]    [Pg.144]    [Pg.106]    [Pg.765]    [Pg.78]    [Pg.418]    [Pg.534]    [Pg.1128]    [Pg.1216]    [Pg.332]    [Pg.195]    [Pg.163]    [Pg.165]    [Pg.67]    [Pg.89]    [Pg.89]    [Pg.90]    [Pg.99]    [Pg.331]    [Pg.151]    [Pg.213]    [Pg.94]    [Pg.527]    [Pg.37]    [Pg.617]    [Pg.29]    [Pg.408]    [Pg.1285]    [Pg.32]    [Pg.269]    [Pg.263]    [Pg.93]   
See also in sourсe #XX -- [ Pg.270 ]




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Acid-sensitive substrates, hydrogenation

Asymmetric Hydrogenation of Standard Test Substrates

Asymmetric hydrogenation substrate complexes

Asymmetric hydrogenation with neutral substrates

Enantioselective Hydrogenation of Prochiral Substrates

Enantioselective hydrogenation substrates

Homogeneous Hydrogenation of Organic Substrates

Hydrogen Abstraction from Substrate

Hydrogen as substrate

Hydrogen from unactivated substrates

Hydrogen permeation substrate effect

Hydrogen peroxide, as substrate

Hydrogen production high substrate concentration

Hydrogen production substrate composition

Hydrogenation amino acid substrates

Hydrogenation high substrate/catalyst ratios

Hydrogenation kinetic equations, substrate concentration

Hydrogenation of Interesting Substrates and Renewable Sources

Hydrogenation of Olefinic Substrates

Hydrogenation olefinic substrates

Hydrogenation rates, substrate dependence

Hydrogenation substrates and transition metal catalysts

Interference of Hydrogen Peroxide Dissociation and Substrate Oxidation Reactions

Ketone hydrogenation substrates

Ligands for Iridium-catalyzed Asymmetric Hydrogenation of Challenging Substrates

Model substrates hydrogenation

Myeloperoxidase hydrogen peroxide substrate

Reactions with direct transfer of hydrogen between nicotinamide coenzyme and substrate

Substrate-Directive Diastereoselective Hydrogenation

Substrate-controlled hydrogenation

Substrate-directive hydrogenation

Substrates conjugate reduction, catalytic hydrogenation

Transfer hydrogenation ketone substrates

Transfer hydrogenation olefin substrates

Unsaturated model substrates hydrogenation

Unsaturated substrates hydrogenation

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