Posebna izdanja (Srpdka kraljevska akademija), Том 237 |
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Страница 15
... resistant to hydrogenation by other methods or that do not respond to characteristic reagents for the carbonyl group , are readily reduced by lithium aluminum hydride to the corresponding alcohols . 81 , 82 125-133 , 1062 , 1067 , 1084 ...
... resistant to hydrogenation by other methods or that do not respond to characteristic reagents for the carbonyl group , are readily reduced by lithium aluminum hydride to the corresponding alcohols . 81 , 82 125-133 , 1062 , 1067 , 1084 ...
Страница 16
... resistant to attack by lithium aluminum hydride187 ( see VIII , 1 ) . Halogen ketones and halogen aldehydes are reduced without hydrogenolysis of the halogen to the corresponding halogen alco- hols ; 83 , 85 , 90 , 93 , 16 V. M. Mićović ...
... resistant to attack by lithium aluminum hydride187 ( see VIII , 1 ) . Halogen ketones and halogen aldehydes are reduced without hydrogenolysis of the halogen to the corresponding halogen alco- hols ; 83 , 85 , 90 , 93 , 16 V. M. Mićović ...
Страница 62
... resistant to hydride reduction , 460 in contrast to its substituted 1030 and octahydro deriva- tives , 662 , 965 , 1030 , 1643 which react normally with lithium aluminum hydride . It has been reported that the ester group in 3 ...
... resistant to hydride reduction , 460 in contrast to its substituted 1030 and octahydro deriva- tives , 662 , 965 , 1030 , 1643 which react normally with lithium aluminum hydride . It has been reported that the ester group in 3 ...
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