Preparation combination treatment

Deep pink polycrystalline solid Rup4 has been prepared by treatment of AsFs with [Ru(F)g] in anhydrous HF solution." A combination of X-ray synchrotron and neutron powder diffraction data reveal that each Ru-atom has six F ligands with an octahedral framework, four in the same plane, each shared with another Ru-atom, to form a puckered-sheet array (Ru—F (bridge) = 2.00 A and 2.00 A, Ru—F—Ru 133°). ... 

Titanium in a low valence state, as prepared by treatment of solutions of titanium trichloride with potassium [206] or magnesium [207] in tetrahydro-furan or with lithium in dimethoxyethane [206], deoxygenates ketones and effects coupling of two molecules at the carbonyl carbon to form alkenes, usually a mixture of both stereoisomers. If a mixture of acetone with other ketones is treated with titanium trichloride and lithium, the alkene formed by combination of acetone with the other ketone predominates over the symmetrical alkene produced from the other ketone [20(5] Procedure 39, p.215). 

Due to an unusual relationship between its sorptive properties and the molecular weight of substances adsorbed, Enterosgel practically does not bind medicinal compounds administered orally, because in the majority of cases they have molecular weight below 1,500 Da. This characteristic of Enterosgel opens many prospective avenues for its use in combined treatment of chronic diseases associated with prolonged use of toxic pharmacologic preparations. 

A generalized representation of cellulose ethers is Cell—OR, wherein the ether group (R) is alkyl, aromatic, heteroalkyl, heterocyclic, or other substituent, including ether groups bearing other functional groups. Cellulose ethers with mixed ether substituents also have been prepared by treatment with two or more reactants, either in combination or in sequence. 

This concerns combined treatments used before the peels as well as the cosmeceuticals or pharmaceutical products used by the patient (see above). Medium-term preparation starts 2-4 weeks before a peel. 

Catalyst prepared by treatment of the copper(II) bis(chelate) complex with phenylhydrazine. The combination of 12 with copper(I) /er/-butoxide gave very low ee values. ... 

Antacids neutralize gastric acid, inactivate pepsin, and bind bile salts. Aluminum-containing antacids also suppress HP and enhance mucosal defense. ° G1 adverse effects are most common with antacids and are dose dependent. Magnesium salts cause an osmotic diarrhea, whereas aluminum salts cause constipation. Diarrhea usually predominates with magnesium/aluminum preparations. Aluminum-containing antacids (except aluminum phosphate) form insoluble salts with dietary phosphorus and interfere with phosphorus absorption. Hypophosphatemia occurs most often in patients with low dietary phosphate intake (e.g., malnutrition or alcoholism). Combined treatment with sucralfate may amplify the hypophosphatemia and the potential for aluminum toxicity (see section on sucralfate). 

Diarylsulfones are easily prepared by treatment of the thallium compound with copper(II) benzenesulfinate generated in situ by the combination of copper(II) sulfate with an excess of sodium benzenesulfinate. 146... 

Synergistic action of colistin and polymyxin in combination with other antibiotics in vitro and in vivo has been reported by several investigators " . In clinical application the effect of these combinations seems to be more a broadening of the antimicrobial spectrum than a synergistic interaction. Several salts and derivatives of both colistin and polymyxin have been reported. Commercially available are the sulphates and also recently the sodium sulphomethyl derivatives which are prepared by treatment of the free bases of polymyxin and colistin with formaldehyde and sodium bisulphite . These derivatives have a lower toxicity than the sulphates, however, and their in vitro antimicrobial activity is also reduced. 

The electrophilic addition of arylbis(arylthio)sulfonium salts to glycals in the presence of alcohols, directly provide 2-thio-(5-glycosides with good stereoselectivity [162]. Stereoselective syntheses of [5-glycosides were also obtained from the reaction of 1,2-trans acetoxysele-nides, prepared by treatment of glycals with phenylselenyl chloride and silver acetate, in the presence of trimethylsilyl triflate [163]. Combined application of this method and the trichlo-roacetimidate method (see section 3.3) was suggested for the synthesis of functionalized precursors of the olivomycin C-D-E trisaccharide [164] (Scheme 34). 

Amino-l-nitro-l,2,4-triazole (581), obtained by nitration of 5-amino-triazole with acetyl nitrate, rearranges, on heating, to the nitramino-triazole (582). ° The combined action of sodium hydroxide, potassium iodide, tri-ethylamine, and sodium dihydrogen phosphite on the chloro-nitro-triazole (583) results in a mixture of the rearranged triazole (584), 3-chloro-l,2,4-triazole, and the coupled product (585). The stable betaine (586) has been prepared by treatment of 4-phenyl-1,2,4-triazole with phenacyl bromide, followed by tri-ethylamine. The meso-ionic triazolium thiolate (537 X = S) reacts with chlorine to form the dichloride (587 X = SCU), which has been converted into the betaine (588) by the action of diethyl bromomalonate in the presence of triethylamine. ... 

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