Posebna izdanja (Srpdka kraljevska akademija), Том 237 |
Из књиге
Резултати 1-3 од 37
Страница 15
Srpska akademija nauka i umetnosti. VI ALDEHYDES , KETONES AND QUINONES 1. ALDEHYDES AND KETONES Carbonyl groups are readily reduced by means of lithium aluminum hydride yielding hydroxy compounds ; 3 , 81-124 , 890 , 1042 , 1051— 1053 ...
Srpska akademija nauka i umetnosti. VI ALDEHYDES , KETONES AND QUINONES 1. ALDEHYDES AND KETONES Carbonyl groups are readily reduced by means of lithium aluminum hydride yielding hydroxy compounds ; 3 , 81-124 , 890 , 1042 , 1051— 1053 ...
Страница 19
... carbonyl group and of the double bond , yielding saturated alcohols.3 , 96 , 216 , 217 , 1485 However , as the ethylenic bond is attacked only at a moderate rate at room temperature ( and after the reduction of the carbonyl function ) ...
... carbonyl group and of the double bond , yielding saturated alcohols.3 , 96 , 216 , 217 , 1485 However , as the ethylenic bond is attacked only at a moderate rate at room temperature ( and after the reduction of the carbonyl function ) ...
Страница 25
... carbonyl function , namely a - methyl ketones , are formed as the result of hydro- genolysis of the hydroxymethylene group . 1878 , 1413 Reductones , i . e . compounds containing the enediol- ( a ) -a - carbonyl function ( XLIX ) , as ...
... carbonyl function , namely a - methyl ketones , are formed as the result of hydro- genolysis of the hydroxymethylene group . 1878 , 1413 Reductones , i . e . compounds containing the enediol- ( a ) -a - carbonyl function ( XLIX ) , as ...
Садржај
LITHIUM ALUMINUM HYDRIDE AS A REDUCING AGENT IN | 1 |
III | 7 |
Special Procedures and Preparation of Hydride Solutions | 13 |
други делови (26) нису приказани
Друга издања - Прикажи све
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