Posebna izdanja (Srpdka kraljevska akademija), Том 237 |
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Страница 8
... action of lithium aluminum hydride on boron chloride or boron fluoride , diborane is obtained in quantitative yield.1 , 56 , 61 , 1832-1834 , 1447 Borazole , B , N , H ,, is formed by the reduction of B - trichloroborazole in ether ...
... action of lithium aluminum hydride on boron chloride or boron fluoride , diborane is obtained in quantitative yield.1 , 56 , 61 , 1832-1834 , 1447 Borazole , B , N , H ,, is formed by the reduction of B - trichloroborazole in ether ...
Страница 52
... action of the reducing agent on the hydrogen atoms of the amide group . . The same reduction was previously accomplished either by catalytic hydrogenation in the presence of copper chromite , by elec- trolysis , or by means of sodium ...
... action of the reducing agent on the hydrogen atoms of the amide group . . The same reduction was previously accomplished either by catalytic hydrogenation in the presence of copper chromite , by elec- trolysis , or by means of sodium ...
Страница 71
... action of lithium aluminum deuteride , yielded dl - erythro - 2 - deutero - 1,2 - diphenylethanol ( XII ) in a highly stereospecific reaction.1322 The cis oxide gave the threo isomer , 1322 CH3 H2C IX CH3 H OH X CH3 H. H. 0 -C6H5 LIAID4 ...
... action of lithium aluminum deuteride , yielded dl - erythro - 2 - deutero - 1,2 - diphenylethanol ( XII ) in a highly stereospecific reaction.1322 The cis oxide gave the threo isomer , 1322 CH3 H2C IX CH3 H OH X CH3 H. H. 0 -C6H5 LIAID4 ...
Садржај
LITHIUM ALUMINUM HYDRIDE AS A REDUCING AGENT IN | 1 |
III | 7 |
Special Procedures and Preparation of Hydride Solutions | 13 |
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Acta action of lithium alcohols aldehydes aliphatic alkyl amides amino aromatic attack by lithium carbon atom carbonyl carbonyl group CH₂ CH₂O CH₂OH CH3 CH3 Chem Chemistry and Industry Chim chloride complex compounds containing converted corresponding cyclic derivatives diethyl ether dihydro diol double bond enol epoxides ester group ether solution ethylenic forcing conditions formation functional groups furnishes give H₂C H₂CO H₂O halides halogen Helv heterocyclic Hydride in Organic hydrocarbons hydrogen hydrogenolysis hydrolysis hydroxy hydroxyl group intermediate Karrer ketones lactams lactone LIAIHA lithium aluminum hydride lithium hydride means of lithium mechanism methyl mixture Monatsh nitriles nitro nitrogen nucleophilic obtained olefin optically active oxazolone oxide polar racemic react with lithium reaction reagent reducing agent reductions by lithium ring Rosenkranz saturated solvent steroids sulfinic acids sulfonate sulfonic acids temperatures tertiary tetrahydrofuran unsaturated VIII XVII XVIII XXIII yields