Octanoate activation

Frozen spores of P. roquefortii Methyl ketone from octanoic acid Isoparaffin-water (87/13) After thawing, only external spores are active 20... 

Table 3 indicates that 5%Pt,l%Bi/C is active for three reaction cycles in the selective oxidation of the chosen alcohols. For primary alcohols the use of water as solvent can promote the aldehyde to carboxylic acid reaction (3). This effect is observed in the selective oxidation of 1-octanol where octanoic acid is formed with 97% selectivity in the first cycle dropping to 81% in the third. In the selective oxidation of geraniol only citral is observed as the oxidation product. The presence of the double bond stabilises the aldehyde even in the presence of... 

Synthesis of PHAMCL from fatty acids such as octanoic acid or from the corresponding alkanes such as octane was first detected in P. oleovorans [119]. The alkanes are oxidized to the fatty acids the latter are activated by thiokinases and then degraded via the fatty acid /1-oxidation pathway. Obviously intermediates of this pathway accumulate under conditions favorable for the synthesis of PHA and are subsequently converted into substrates for the PHA synthase. Many reactions for the conversion of an intermediate of the -oxidation cycle into R-(-)-3-hydroxyacyl-CoA were considered. These were ... 

Vinyl octanoate was obtained from TCI (Tokyo, Japan). All other chemicals with the exception of the zeolite beta are available from Sigma Aldrich. The synthesis of a particularly active modification of low-alumina zeolite beta has been described by us. Commercial material, available as samples from, for example, Zeolyst or Siidchemie can be used, but because of excessive acidity may result in up to 15 % of styrene formation. 

How to analyze the phosphate counterion of a known active pharmaceutical compound (API), primaquine diphosphate, is shown as an example. A simplified method was used to demonstrate the feasibility of the method. For this purpose, we prepared three sample solutions and three standard solutions each at 70%, 100%, and 130% of the expected value. Octanoic acid was chosen as internal standard. 

Also for this reaction, namely esterification plus transesterification, mixed oxides, this time acidic in nature, appear to be the most promising alternative. Tungstated zirconia-alumina (WZA), sulfated zirconia-alumina and sulfated tin oxide were shown to be active in the transesterification of soybean oil with methanol at 200-300 °C and in the esterification of n-octanoic acid with methanol at 175-200 °C. Although the order of activities is different for the two reactions, WZA gives high conversions in both readions and it is stable under the reaction conditions [31]. Titania on zirconia, alumina on zirconia and zirconia on alumina also showed good performances [32, 6]. 

Polymerization of the bulky monomer chloral yields an optically active product when one uses a chiral initiator, e.g., lithium salts of methyl (+)- or (—)-mandelate or (R)- or (S)-octanoate [Corley et al., 1988 Jaycox and Vogl, 1990 Qin et al., 1995 Vogl, 2000], The chiral initiator forces propagation to proceed to form an excess of one of the two enantiomeric helices. The same driving force has been observed in the polymerization of triphenyl-methyl methacrylate at —78°C in toluene by initiating polymerization with a chiral complex formed from an achiral initiator such as n-butyllithium and an optically active amine such as (+)-l-(2-pyrrolidinylmethyl)pyrrolidine [Isobe et al., 2001b Nakano and Okamoto, 2000 Nakano et al., 2001]. Such polymerizations that proceed in an unsymmetrical manner to form an excess of one enantiomer are referred to as asymmetric polymerizations [Hatada et al., 2002]. Asymmetric polymerization has also been observed in the radical... 

Sulfated tin oxide (STO) is classified as one of the strongest solid acids (STO calcined at 550°C ranks first among sulfated metal oxides according to the Hammett function scale, Hq value = 18). However, the use of STO has been more limited than that of SZ (calcined at 650°C, Hq value = —16.1) due to preparation difficulties and poor yields. However, new preparation routes are making this catalyst more accessible, and recently its use has become more widespread. In a recent study by Furuta et al., STO was compared to SZ in the esterification of n-octanoic acid with methanol. The STO catalyst showed superior activity compared to SZ at temperatures below 150°C. For instance, STO approached a 100% ester yield at 100°C, while SZ required temperatures as high as 150°C to reached similar yields. 

Lipolysed milk fat was one of the first flavours produced with the help of enzymes. The original process was based on the controlled lipase-catalysed hydrolysis of cream [18]. For instance, Mucor miehei lipase possesses a high selectivity towards flavour-active short-chain fatty acids. Additionally, lipases that prefer long-chain fatty acids or lipases without particular preferences can be found. The free fatty acids produced can be isolated by steam distillation and further purified. Thus, it is possible to obtain pure short-chain fatty acids like butanoic, hexanoic, octanoic and decanoic acid. 

So far it has not been possible to measure the chemical potentials of the components in the mesophases. This measurement is possible, however, in solutions which are in equilibrium with the mesophases. If pure water is taken as the standard state, the activity of water in equilibrium with the D and E phases in the system NaC8-decanol-water is more than 0.8 (4). From these activities in micellar solutions, the activity of the fatty acid salt has sometimes been calculated. The salt is incorrectly treated as a completely dissociated electrolyte. The activity of the fatty acid in solutions of short chain carboxylates has also been determined by gas chromatography from these determinations the carboxylate anion activity can be determined (18). Low CMC values for the carboxylate are obtained (15). The same method has shown that the activity of solubilized pentanol in octanoate solutions is still very low when the solution is in equilibrium with phase D (Figure 10) (15). 

Figure 10. The activity of n-pentanol in micellar solutions of sodium octanoate with solubilized pentanol and in equilibrium with the lamellar mesophase D. The abscissa indicates the mole fraction of sodium octanoate in the system (15).

Table 5.28. Activity of Nafion Catalysts in the Acylation of Anisole with Octanoic Acid376...

Sodium octanoate is the water soluble sodium salt of octanoic (caprylic) acid, but it has no antibacterial or antifungal activity as tested by the same procedures described above, and the results are reported in Table 4.12. 

Table 4.12 Antifungal activity of caprylic acid and sodium octanoate...

An entirely different reaction occurred when 2-(4-diazo-3-oxobutyl)-benzoxazole (239) was treated with Rh(II) octanoate. In addition to undergoing dipolar cycloaddition to produce cycloadduct 241 (20%), the highly stabilized dipole (i.e., 240) formed from the benzoxazole loses a proton to produce the cyclic ketene N,O-acetal 242. This compound reacts further with the activated 7t-bond of DMAD to give zwitterion 243. The anionic portion of 243 then adds to the adjacent carbonyl group, producing a new zwitterionic intermediate 244. In the presence of water, this species is converted to the observed phenolic lactam 245. 

Beers, A. E. W., van Bokhoven, J. A., de Lathouder, K. M., Kapteijn, F. and Moulijn, J. A. Optimization of zeolite Beta by steaming and acid leaching for the acylation of anisole with octanoic acid a structure-activity relation, J. Catal., 2003, 218, 239-248. 

In the context of ternary catalyst systems Throckmorton s pioneering work is worth mentioning although in this study Ce rather than Nd-based catalyst systems were used. For the two catalyst systems Ce octanoate/TIBA/DEAC and Ce octanoate/TIBA/EADC catalyst activities increased up to TiBA/ Ce = 20. Further increases in the TiBA/ Ce-ratios from 20-60 did not result in further activity improvements [34]. For a ternary didymium (Di)-based oc-tanoate catalyst system Witte described a similar dependence. Within the wAl/ Di-range 20-40 significant increases of polymerization rates were reported. Further increases of the nAi//iDi-ratios did not have an additional effect [49]. 

To the present day there is an ongoing search for the magic additive which allows molar mass control of Nd-catalyzed polymerizations without a detrimental effect on polymerization activities. This search is documented in the scientific as well as in the patent literature. In this context ethanol, dihydronaphthaline, chloroform, diethyl aniline, triphenylmethane, octanoic acid, allyl iodide and diallylether were unsuccessfully evaluated [464,465]. Also propylene, oxygen, 1,5-hexadiene, ethyltrichloroacetate and n-butanol resulted in the deactivation of the catalyst system without the desired reduction of molar mass [157]. 

Although heterobimetallic complexes with alkylated rare-earth metal centers were proposed to promote 1,3-diene polymerization via an allyl insertion mechanism, details of the polymerization mechanism and of the structure of the catalytically active center(s) are rare [58,83,118-125]. Moreover, until now, the interaction of the cationizing chloride-donating reagent with alkylated rare-earth metal centers is not well-understood. Lanthanide carboxylate complexes, which are used in the industrial-scale polymerization of butadiene and isoprene, are generally derived from octanoic, versatic, and... 

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