Hydrogenolysis of allylic alcohols with mixed hydride reagent of lithium aluminum hydride-titanium tetrachloride.
نویسندگان
چکیده
منابع مشابه
Regeneration of lithium aluminum hydride.
Lithium aluminum hydride (LiAlH(4)) is a promising compound for hydrogen storage, with a high gravimetric and volumetric hydrogen density and a low decomposition temperature. Similar to other metastable hydrides, LiAlH(4) does not form by direct hydrogenation at reasonable hydrogen pressures; therefore, there is considerable interest in developing new routes to regenerate the material from the ...
متن کاملReduction of Halomethanes with Lithium Aluminum Hydride
A study has been made of t he reactions of lithium aluminum hydride with methyl bromide, methylene chloride, meth ylene bromide, methylene iodide, chloroform, bromoform, and carbon t etrachloride. Except for hydrogen and unreacted h alida, essentia lly pure methane was formed in each case. The amount of hydrogen evolved increased with the n umber of halogen atoms in the molecule, reaching a max...
متن کاملAluminum Hydride Chemistry
Anion photoelectron spectroscopy and density functional theory were employed to study aluminum hydride clusters, AlnHm (4 e n e 8, 0 e m e 10). Photoelectron spectra revealed that Al4H4, Al4H6, and a family of species with general formula AlnHn+2 (5 e n e 8) have small adiabatic electron affinities and large HOMO-LUMO gaps (ranging from 0.5 to 1.9 eV) relative to those of their stoichiometric n...
متن کاملStark deceleration of lithium hydride molecules
We describe the production of cold, slow-moving LiH molecules. The molecules are produced in the ground state using laser ablation and supersonic expansion, and 68% of the population is transferred to the rotationally excited state using narrowband radiation at the rotational frequency of 444 GHz. The molecules are then decelerated from 420 m/s to 53 m/s using a 100 stage Stark decelerator. We ...
متن کاملFacile synthesis of a genuinely alkane-soluble but isolable lithium hydride transfer reagent.
1-Lithio-2-butyl-1,2-dihydropyridines, typically formed as intermediates in the nucleophilic substitution (addition/elimination) of pyridine with (n- or t-)butyl lithium, have been isolated and comprehensively characterized. The linear substituted isomer is polymeric while the branched substituted isomer is a cyclotrimer. The lower oligomerization of the latter complex confers exceptional hexan...
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ژورنال
عنوان ژورنال: Chemical and Pharmaceutical Bulletin
سال: 1976
ISSN: 0009-2363,1347-5223
DOI: 10.1248/cpb.24.825