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Reaction facilitating

Of all the work described in this thesis, this discovery is probably the most significant. Given the fact that the arene - arene interactions underlying the observed enantioselectivity of ftie Diels-Alder reactions described in Chapter 3 are also encountered in other organic reactions, we infer that, in the near future, the beneficial influence of water on enantioselectivity can also be extended to these transformations. Moreover, the fact that water can now be used as a solvent for enantioselective Lewis-add catalysed reactions facilitates mechanistic studies of these processes, because the number of equilibria that need to be considered is reduced Furthermore, knowledge and techniques from aqueous coordination chemistry can now be used directly in enantioselective catalysis. [Pg.162]

The decomposition kinetics of mercury fulminate [725] are significantly influenced by ageing, pre-irradiation and crushing these additional features of reaction facilitated interpretation of the observations and, in particular, the role of intergranular material in salt breakdown. Following a slow evolution of gas ( 0.1%) during the induction period, the accelerator process for the fresh salt obeyed the exponential law [eqn. (8)] when a < 0.35. The induction period for the aged salt was somewhat shorter and here the acceleratory process obeyed the cube law [eqn. (2), n = 3] and E = 113 kj mole-1. [Pg.166]

Diels-Alder Reaction Facilitated by Special Physical and Chemical Methods... [Pg.143]

Diels-Alder Reaction Facilitated by Physical and Chemical Methods 155 Table 4.8 o-Quinone ultrasound-assisted Diels-Alder reactions... [Pg.155]

Linking the ketone and carboxylic acid components together in an Ugi reaction facilitates the synthesis of pyrrolidinones amenable to library design. The three-component condensation of levulinic acid 30, an amine and isocyanide proceeds under microwave irradiation to give lactams 31 [65]. The optimum conditions were established by a design of experiments approach, varying the equivalents of amine, concentration, imine pre-formation time, microwave reaction time and reaction temperature, yielding lactams 31 at 100 °C in poor to excellent yield, after only 30 min compared to 48 h under ambient conditions (Scheme 11). [Pg.41]

The reversible formation of a complex by Ni ions and the bi dentate ligand pyridine-2-azo-p-dimethylaniline is a simple and thus reliable reaction, not accompanied by side reactions [17]. Kinetic rate law and rate constants for the reaction are known. The time demand of the reaction fits the short time scales typical for micro reactors. The strong absorption and the strong changes by reaction facilitate analysis of dynamic and spatial concentration profiles. [Pg.565]

More recently, a number of different copolymer structures have been prepared from butadiene and styrene, using modified organolithiums as polymerization initiators ( 4). Organolithium initiated polymerizations have gained prominence because stereo-control is combined with excellent polymerization rates, and the absence of a chain termination reaction facilitates control of molecular weights and molecular weight distributions ( 5). [Pg.74]

Heterogeneous reactions facilitated by supported reagents on inorganic oxide surfaces have received attention in recent years, both in the laboratory as well as in industry. Although the first description of the surface-mediated chemical transformation dates back to 1924 [13], it was not until almost half a century later that the technique received extensive attention with the appearance of several reviews, books and account articles [14—22],... [Pg.181]

Displacement of the bound ketone by H2 was directly observed by NMR (Eq. (37)), and an approximate equilibrium constant was determined. The cationic tungsten complex can also be used for catalytic hydrosilylation of ketones. In the case of catalytic hydrosilylation of abphatic substrates using HSiEt3, the catalyst precipitates at the end of the reaction, facilitating recycle and reuse [66],... [Pg.185]


See other pages where Reaction facilitating is mentioned: [Pg.360]    [Pg.171]    [Pg.118]    [Pg.326]    [Pg.40]    [Pg.234]    [Pg.123]    [Pg.615]    [Pg.3]    [Pg.497]    [Pg.329]    [Pg.520]   
See also in sourсe #XX -- [ Pg.342 ]




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