Posebna izdanja (Srpdka kraljevska akademija), Том 237 |
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... diethyl ether , tetra- hydrofuran and methylal , less so in other aliphatic and cyclic ethers with higher boiling points , and insoluble in benzene , in toluene , in chloroform and in saturated aliphatic hydrocarbons . The approximate ...
... diethyl ether , tetra- hydrofuran and methylal , less so in other aliphatic and cyclic ethers with higher boiling points , and insoluble in benzene , in toluene , in chloroform and in saturated aliphatic hydrocarbons . The approximate ...
Страница 21
... diethyl ether solution at 35 ° , gives 75 % of the partially hydrogenated ketone ( XXIV ) and 12—17 % of the hydro- genolysis product ( XXVI ) . In boiling dioxane , 60-65 % of the ethyl- enic ketone ( XXIV ) is obtained and only a ...
... diethyl ether solution at 35 ° , gives 75 % of the partially hydrogenated ketone ( XXIV ) and 12—17 % of the hydro- genolysis product ( XXVI ) . In boiling dioxane , 60-65 % of the ethyl- enic ketone ( XXIV ) is obtained and only a ...
Страница 181
... Diethyl ether , importance of in lith- ium aluminum hydride reduc- tions , 135 Diethyl 2,6 - lutidine - 3,5 - dicarboxyl- ate , 128 selective reduction of one ester group , 40 Diethylmercury , 7 Diethyl oxalate , 38 partial reduction of ...
... Diethyl ether , importance of in lith- ium aluminum hydride reduc- tions , 135 Diethyl 2,6 - lutidine - 3,5 - dicarboxyl- ate , 128 selective reduction of one ester group , 40 Diethylmercury , 7 Diethyl oxalate , 38 partial reduction of ...
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