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Preparation and Synthesis

Preparation and synthesis routes of fluoride-containing apatites... [Pg.280]

PREPARATION AND SYNTHESIS ROUTES OF FLUORIDE-CONTAINING APATITES... [Pg.306]

Limitations of X-ray methods. If it were possible to find the structure of every crystalline substance in this way, chemists would no longer have to spend their time in deducing the structures of new substances by more or less indirect methods they could turn all their energies to preparation and synthesis. In the future it may well be possible to determine the structure of any crystal by X-ray methods without chemical evidence of any sort, but at the present time there are certain difficulties which restrict the scope of such methods. [Pg.5]

The preparation and synthesis of the product to be purified are tasks requiring the highest chemical skills. Re-crystallisation, distillation, fusion, flotation and so on, are all tools, when repeatedly applied, to achieve basic purity. Preparative liquid chromatography (adsorption mode or ion exchange) achieves the purification processes. During and at the end of the preparation and purification process, analytical methods are applied to verify the degree of purity obtained. When a sufficient purity is achieved, it is possible to start the certification measurements to quantify the purity and its uncertainty. Both categories listed above have to be chased. [Pg.168]

Preparation and Synthesis of Amino Sugars. Lobster and crab shells, which consist of calcium carbonate, chitin, and protein material, are hydrolyzed... [Pg.468]

BIA 07] Bianchini J.R., Satto K., Balin T.B. et al, Thymine-based, Water-soluble Phototerpolymers Their Preparation and Synthesis , Journal of Polymer Science Part A Polymer Chemistry, vol. 45, pp. 1296-1303, 2007. [Pg.316]

The conversion of the Chemlnform weekly abstracting service supporting recent publications dealing with methods of preparation and synthesis in organic, organometallic, and inorganic chemistry is described by Gasteiger. The wealth of information on chemical reactions can only be made available in a reaction database. A recent publication describes new developments in this reaction database - especially in the... [Pg.947]

The LCA Process diverged from the traditional design of ammonia plants in a radical way, as it replaced the integrated process with a core unit containing all the key gas preparation and synthesis processes (gas desulfurization, reforming, shift conversion, methanation, and synthesis) and a separate utility area. LCA hydrodesulfurization of natural gas is done at a low temperature, and the primary reformer... [Pg.127]

M.p. 190-192 C. The enolic form of 3-oxo-L-gulofuranolactone. It can be prepared by synthesis from glucose, or extracted from plant sources such as rose hips, blackcurrants or citrus fruits. Easily oxidized. It is essential for the formation of collagen and intercellular material, bone and teeth, and for the healing of wounds. It is used in the treatment of scurvy. Man is one of the few mammals unable to manufacture ascorbic acid in his liver. Used as a photographic developing agent in alkaline solution. [Pg.43]

The telomer 145 of nitroethane was used for the synthesis of recifeiolide (148)[121], The nitro group was converted into a hydroxy group via the ketone and the terminal double bond was converted into iodide to give 146. The ester 147 of phenythioacetic acid was prepared and its intramolecular alkylation afforded the 12-membered lactone, which was converted into recifeiolide (148),... [Pg.445]

SYNTHESIS OF CARBOXYLIC ACIDS BY THE PREPARATION AND HYDROLYSIS OF NITRILES... [Pg.808]

Among the methods for preparing carboxylic acids carboxylation of a Grignard reagent and preparation and hydrolysis of a nitrile convert RBr to RCO2H The malonic ester synthesis converts RBr to RCH2CO2H... [Pg.897]

Preparation. The synthesis of OF2 was first achieved by the electrolysis of molten KHF2 in the presence of water (37). The electrolysis of aqueous HF in the presence of O2 and was also found to produce OF2 (38—40). [Pg.220]

Historically, the discovery of one effective herbicide has led quickly to the preparation and screening of a family of imitative chemicals (3). Herbicide developers have traditionally used combinations of experience, art-based approaches, and intuitive appHcations of classical stmcture—activity relationships to imitate, increase, or make more selective the activity of the parent compound. This trial-and-error process depends on the costs and availabiUties of appropriate starting materials, ease of synthesis of usually inactive intermediates, and alterations of parent compound chemical properties by stepwise addition of substituents that have been effective in the development of other pesticides, eg, halogens or substituted amino groups. The reason a particular imitative compound works is seldom understood, and other pesticidal appHcations are not readily predictable. Novices in this traditional, quite random, process requite several years of training and experience in order to function productively. [Pg.39]

Pentenamer Ionomers. Unsaturated polypentenamer elastomers have been derivatized by post-synthesis reactions (72—74). Phosphonate, thioglycolate, sulfonate, and carboxylate derivatives have been prepared and converted into ionomers. [Pg.409]

Synthesis Gas Preparation Processes. Synthesis gas for ammonia production consists of hydrogen and nitrogen in about a three to one mole ratio, residual methane, argon introduced with the process air, and traces of carbon oxides. There are several processes available for synthesis gas generation and each is characterized by the specific feedstock used. A typical synthesis gas composition by volume is hydrogen, 73.65% nitrogen, 24.55% methane, <1 ppm-0.8% argon, 100 ppm—0.34% carbon oxides, 2—10 ppm and water vapor, 0.1 ppm. [Pg.340]

Since this original synthesis, a great number of improvements (191—201) have been made in the stereoselective preparation and derivatization of the CO-chain precursor, in cuprate reagent composition and preparation, in protecting group utilization, and in the preparation and resolution of hydroxycyclopentenones. Illustration of some of the many improvements are seen in a synthesis (202) of enisoprost, a PGE analogue. The improvements consist of a much more efficient route to the enone as well as modifications in the cuprate reactions. Preparation of the racemic enone is as follows ... [Pg.161]

Quaternary ammonium alkyl ethers are prepared similarly an alkaline starch is reacted with a quaternary ammonium salt containing a 3-chloto-2-hydtoxyptopyl or 2,3-epoxyptopyl radical. Alternatively, such derivatives can be prepared by simple quaternization of tertiary aminoalkyl ethers by reaction with methyl iodide. Sulfonium (107) and phosphonium (108) starch salts have also been prepared and investigated. Further work has explained the synthesis of diethyl aminoethyl starch (109) as well as the production of cationic starches from the reaction of alkaline starch with... [Pg.345]

Alternatively, various 4-substituted derivatives have been prepared via synthesis of amino acid (68) by reaction of the anion formed from protected glycine and an appropriately substituted Schiff base. [Pg.70]

Stmctural variations of the reagents used in these reactions have been a primary source of progress in dye synthesis. Acetylenic reagents for cyanine dye synthesis include the weU-known acetylenic quartemary salts as general electrophilic reagents for the preparation of carbocyanine dyes. A number of tautomeric pairs of acetylenic dyes have been prepared and their tautomeric equiUbria determined (dyes (26a), (26b)) (29). [Pg.395]

Cyclopentadiene itself has been used as a feedstock for carbon fiber manufacture (76). Cyclopentadiene is also a component of supported metallocene—alumoxane polymerization catalysts in the preparation of syndiotactic polyolefins (77), as a nickel or iron complex in the production of methanol and ethanol from synthesis gas (78), and as Group VIII metal complexes for the production of acetaldehyde from methanol and synthesis gas (79). [Pg.435]

If the technical staff from the client company recognizes that a toller may be asked to perform new analyses and make operating decisions based upon the results, the client may help the toller develop the needed procedures and skills required to make these decisions. Typically a round robin laboratory qualification exercise will be performed. Samples of known standards and unknown concentrations of the materials to be analyzed for the toll will be prepared and sent to both laboratories. This can help ensure that equipment calibration is synchronized and that the toller is capable of performing accurate measurements. In some cases, the toller may be the party with the chemical, process, or synthesis specific expertise. [Pg.83]

S. V. Ley, l.R. Baxendale, G. Brusotti, M. Caldarelli, A. Massi and M. Nesi, Solid-supported Reagents for Multi-step Organic Synthesis Preparation and Application, II Farmaco 57 321-330 2002. [Pg.78]

Y2 Cg2 denotes two Y atoms inside a Cg2 fullerene [19], Thus far, only small quantities of endohedrally-doped fullerenes have been prepared and only limited investigations of endohedrally-doped crystalline materials have been reported but steady progress is being made both in synthesis and in properties measurements [20]. [Pg.38]


See other pages where Preparation and Synthesis is mentioned: [Pg.18]    [Pg.3]    [Pg.134]    [Pg.421]    [Pg.18]    [Pg.3]    [Pg.134]    [Pg.421]    [Pg.136]    [Pg.370]    [Pg.416]    [Pg.469]    [Pg.298]    [Pg.298]    [Pg.474]    [Pg.83]    [Pg.243]    [Pg.48]    [Pg.325]    [Pg.133]    [Pg.88]    [Pg.153]    [Pg.73]    [Pg.355]    [Pg.507]    [Pg.1]    [Pg.81]   


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