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Strategy phosphates

Alternative Processes. Because of the large quantity of phosphate rock reserves available worldwide, recovery of the fluoride values from this raw material source has frequently been studied. Strategies involve recovering the fluoride from wet-process phosphoric acid plants as fluosiUcic acid [16961-83-4] H2SiFg, and then processing this acid to form hydrogen fluoride. [Pg.197]

We are familiar with several examples of chemical activation as a strategy for group transfer reactions. Acetyl-CoA is an activated form of acetate, biotin and tetrahydrofolate activate one-carbon groups for transfer, and ATP is an activated form of phosphate. Luis Leloir, a biochemist in Argentina, showed in the 1950s that glycogen synthesis depended upon sugar nucleotides, which may be... [Pg.755]

Phosphate should ideally be added continuously, direct to the boiler shell or steam drum, and in proportion to FW consumption. Where this is not possible and the phosphate is added to the feedline, several program options exist to minimize the potential for feedline blockage. The use of an alternate strategy is particularly important where an economizer is present. Options include ... [Pg.424]

The in situ precipitation route towards obtaining composites of polymer and calcium phosphate is similar to the strategy employed in naturally occurring biocomposites and well may prove a viable method for the synthesis of bone substitutes. [Pg.173]

Phosphonate analogs to phosphate esters, in which the P—0 bond is formally replaced by a P—C bond, have attracted attention due to their stability toward the hydrolytic action of phosphatases, which renders them potential inhibitors or regulators of metabolic processes. Two alternative pathways, in fact, may achieve introduction of the phosphonate moiety by enzyme catalysis. The first employs the bioisosteric methylene phosphonate analog (39), which yields products related to sugar 1-phosphates such as (71)/(72) (Figure 10.28) [102,107]. This strategy is rather effective because of the inherent stability of (39) as a replacement for (25), but depends on the individual tolerance of the aldolase for structural modification close... [Pg.295]

Other anionic phosphates 27a-27e, 28, 29, and 30 (Fig. 6), which contain both P-C and P-0 bonds, have been reported since 1997. In these cases, as shown by Akiba, Kawashima and Holmes, the synthetic strategy is slightly different as P-C bonds usually need to be formed prior to P-0 ones. [Pg.10]

Successful strategies for generating complexes of the di(terf-butyl)phosphate ligand primarily focus on the use of H0P(0)(0 Bu)2 as a reagent. As with the related siloxide species, all synthetic manipulations must be performed under inert conditions to avoid hydrolysis of the M - O - P linkages. Complexes of the - 02P(0 Bu)2 ligand are useful precursors to M/P/0 oxide materials. [Pg.84]

Adequate levels of lime, phosphate and potash in the soil are especially important for organic dairy farmers, because these nutrients are essential for healthy white clover. The supply of these nutrients and general manure strategy is covered fully by Newton (1993). [Pg.41]

Figure 7 A novel, phosphate ester linking strategy [22] was used in the synthesis of phenyl phosphate-containing compound libraries, accomplished in 96-deepwell reaction blocks [23], Rigid, nonpeptide templates (A-group) and pY+3 substituents (B-group) satisfied the diversity sites of the molecules. Figure 7 A novel, phosphate ester linking strategy [22] was used in the synthesis of phenyl phosphate-containing compound libraries, accomplished in 96-deepwell reaction blocks [23], Rigid, nonpeptide templates (A-group) and pY+3 substituents (B-group) satisfied the diversity sites of the molecules.
The use of the phenyl phosphate group as both a solid support attachment site and a crucial binding element represents what has been referred to as a pharmacophore-linking strategy [26]. We explored a variety of phenyl phosphate tether functionalities to provide resins varying in substitution pattern and in chemical flexibility (Scheme 1 and Table 4) [22]. All phenyl phosphate resins were synthesized in batch quantities of 20 g or more. Resin synthesis began with the addition of either /mnethoxy-benzyl alcohol or benzyl alcohol to commercially available bis(diisopro-pylamino)chlorophosphine, followed by addition of the diversity phenol [(Ri)-OFl, DIAT (diisopropylamino tetrazole)]. Displacement of the... [Pg.45]

An alternative system proved to be both simpler and more user friendly (Unger et al., 2004 Machtejevas et al., 2006). Thus far we have used this configuration to analyze human plasma, sputum, urine, cerebrospinal fluid, and rat plasma. For each particular analysis we set up an analytical system based on a simple but specific strategy (Figure 9.5). The analysis concept is based on an online sample preparation and a two-dimensional LC system preseparating the majority of the matrix components from the analytes that are retained on a RAM-SCX column followed by a solvent switch and transfer of the trapped peptides. The SCX elution used five salt steps created by mixing 20 mM phosphate buffer (pH 2.5) (eluent Al) and 20 mM phosphate buffer with 1.5 M sodium chloride (eluent Bl) in the following proportions 85/15 70/30 65/45 45/55 0/100 with at the constant 0.1 mL/min flow rate. Desorption of the... [Pg.214]

Abdel-Khalek, N. A. Evaluation of flotation strategies for sedimentary phosphates with siliceous and carbonates gangues. Miner. Eng. 2000, 13, 789-793. [Pg.798]

This same type of modification strategy also can be used to create highly reactive groups from functionalities of rather low reactivity. For instance, carbohydrate chains on glycoproteins can be modified with sodium periodate to transform their rather unreactive hydroxyl groups into highly reactive aldehydes. Similarly, cystine or disulfide residues in proteins can be selectively reduced to form active sulfhydryls, or 5 -phosphate groups of DNA can be transformed to yield modifiable amines. [Pg.66]


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See also in sourсe #XX -- [ Pg.19 ]




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Strategy synthesis with glycosyl phosphates

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