Posebna izdanja (Srpdka kraljevska akademija), Том 237 |
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Страница 1
... reductions by lithium aluminum hydride proceed readily and smoothly at room temperature without side reactions ; 5 ) it can be used ... LITHIUM ALUMINUM HYDRIDE AS A REDUCING AGENT IN GANIC CHEMISTRY Advantages of Lithium Aluminum Hydride.
... reductions by lithium aluminum hydride proceed readily and smoothly at room temperature without side reactions ; 5 ) it can be used ... LITHIUM ALUMINUM HYDRIDE AS A REDUCING AGENT IN GANIC CHEMISTRY Advantages of Lithium Aluminum Hydride.
Страница 2
... Lithium aluminum hydride and the Grignard reagent appear to differ principally in the more aggressive behavior of the hydride , resulting in a lessening of side reactions and of steric influences . For that reason the hydride reductions ...
... Lithium aluminum hydride and the Grignard reagent appear to differ principally in the more aggressive behavior of the hydride , resulting in a lessening of side reactions and of steric influences . For that reason the hydride reductions ...
Страница 134
... reductions with lithium aluminum hydride is actually a series of complex aluminohydride anions Al ( OR ) He , where n progresses from 0 to 4 during the course of a reaction , and which act as carriers for hydride ion.86 , 695 It is by ...
... reductions with lithium aluminum hydride is actually a series of complex aluminohydride anions Al ( OR ) He , where n progresses from 0 to 4 during the course of a reaction , and which act as carriers for hydride ion.86 , 695 It is by ...
Садржај
LITHIUM ALUMINUM HYDRIDE AS A REDUCING AGENT IN | 1 |
III | 7 |
Special Procedures and Preparation of Hydride Solutions | 13 |
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Чести термини и фразе
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