Samarium-titanium chloride

Magnesium, 235 Samarium(II) iodide, 270 Titanium(IV) chloride, 304 Addition reactions to carbonyl groups—Addition of functionalized CARBON NUCLEOPHILES (see also Aldol reaction and other specific condensation reactions, Meth-ylenation, Peterson Olefination, Refor-matsky reaction, Wittig reaction, Wittig-Horner reaction)... 

Diphenylphosphine)lithium, 126 Nickel boride, 197 Samarium(II) iodide, 270 to 1,2-disubstituted compounds B-3-Pinanyl-9-borabicyclo-[3.3.1]nonane, 249 Titanium(III) chloride, 302 of phosphorus compounds Lithium aluminum hydride-Cerium(III) chloride, 159 of sulfoxides and sulfones Sodium iodide-Boron trifluoride ether-ate, 282... 

Reductive coupling of carbonyls to alkenes Titanium(IV) chloride-Zinc, 310 of carbonyls to pinacols Titanium(III) chloride, 302 Titanium(IV) chloride-Zinc, 310 of other substrates Samarium(II) iodide, 270 Reductive cyclization 2-(Phenylseleno)acrylonitrile, 244 Tributylgermane, 313 Tributyltin hydride, 316 Triphenyltin hydride, 335 Trityl perchlorate, 339 Reductive hydrolysis (see Hydrolysis) Reductive silylation Chlorotrimethylsilane-Zinc, 82... 

Norephedrine, 200 Organoaluminum reagents, 202 Organotitanium reagents, 213 9-(Phenylseleno)-9-borabicyclo-[3.3.1]nonane, 245 Tin(II) chloride, 298 Titanium(IV) chloride, 304 Trityllithium, 338 Trityl perchlorate, 339 Zinc chloride, 349 By other reactions Chloromethyl ethyl ether, 75 Dibutyltin oxide, 95 Samarium(II) iodide, 270 Tributyltin hydride, 316 Hydroxy amides a-Hydroxy amides... 

Fundamental studies have been reported using the cationic liquid ion exchanger di(2-ethylhexyl) phosphoric acid in the extraction of uranium from wet-process phosphoric acid (H34), yttrium from nitric acid solution (Hll), nickel and zinc from a waste phsophate solution (P9), samarium, neodymium, and cerium from their chloride solutions (12), aluminum, cobalt, chromium, copper, iron, nickel, molybdenum, selenium, thorium, titanium, yttrium, and zinc (Lll), and in the formation of iron and rare earth di(2-ethylhexyl) phosphoric acid polymers (H12). Other cationic liquid ion exchangers that have been used include naphthenic acid, an inexpensive carboxylic acid to separate copper from nickel (F4), di-alkyl phosphate to recover vanadium from carnotite type uranium ores (M42), and tributyl phosphate to separate rare earths (B24). 

Apart from the compounds already mentioned, vanadium, manganese, and cobalt chlorides, tetra-alkoxy derivatives of titanium, acetylacetonates of V, Cr, Mo, Mn, and Ni, Cp derivatives of Zr and Nb, and triphenyl phosphine complexes of Ti and Fe were found to be active. Later lanthanide complexes were included in the list of dinitrogen-reducing systems, the most effective being compounds of samarium and yttrium. 

The same reaction products are obtained from epoxides and TMS-CN in the presence of aluminum al-koxides, samarium, cerium or lanthanum chlorides as well as titanium tetraisopropanoate, which may all be considered comparatively hard Lewis acids. On the other hand various groups demonstrated that softer Lewis acids like zinc, tin and palladium dichloride may give rise to isocyanides (Scheme 15). 

Samarium. 14,275 17,301 Reductions. In the re included. For example, iodii aryl azides, and sodium alk Titanium(rV) chloride an e.g., in the transformation of amines, respectively. 

Metal chloride complexes (59) with structures analogous to that of the samarium complex (50) have been obtained by the reaction of (57) with titanium or zirconium tetrachlorides via elimination of LiCl. Equimolar reaction of (57) and CrCl2(thf)2 has been shown to yield binuclear chromium complex (60), whilst reaction with a twofold excess of CrCl2(thf)2 affords a partially substituted tetranuclear complex (61). ... 

Samarium selenides. Reductive cleavage of ArSeSeAr by samarium is catalyzed by a great number of metal halides bismuth(III) chloride, cadmium chloride, chromium(IIl) chloride, cobalt(II) chloride, potassium iodide, and titanium(lV) chloride. The resulting samarium arylselenides readily react with various organic halides. 

Many methods are available for the removal of oxygen from A -oxides, samarium iodide, chromous chloride, stannous chloride with low-valent titanium, ammonium formate with palladium, and catalytic hydrogenation all do the job at room... 

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