Posebna izdanja (Srpdka kraljevska akademija), Том 237 |
Из књиге
Резултати 1-3 од 59
Страница 180
... containing carbon isotopes , 30 containing conjugated double bonds , 33 hydrogenolysis of , 31 , 77 , 78 reduction to aldehydes , 31 , 32 showing steric hindrance , 29 , 30 , 33 , 45 Cellulose , nitrates , 101 Cetylphosphate , 101 ...
... containing carbon isotopes , 30 containing conjugated double bonds , 33 hydrogenolysis of , 31 , 77 , 78 reduction to aldehydes , 31 , 32 showing steric hindrance , 29 , 30 , 33 , 45 Cellulose , nitrates , 101 Cetylphosphate , 101 ...
Страница 185
... containing conjugated double bonds , 19 containing isotopic carbon , 17 formation of , 42-44 , 89 , 107 , 108 mechanism of reduction of , 26 , 133-135 see also Carbonyl groups and Ali- cyclic ketones Keto nitriles , splitting of , 85 ...
... containing conjugated double bonds , 19 containing isotopic carbon , 17 formation of , 42-44 , 89 , 107 , 108 mechanism of reduction of , 26 , 133-135 see also Carbonyl groups and Ali- cyclic ketones Keto nitriles , splitting of , 85 ...
Страница 192
... containing bonds , 33 conjugated double containing the styryl rest , 33 , 121-123 Unsaturated alcohols , from 1,3 - di- ketones , 24 from a - hydroxymethylene ketones , 24 , 25 from B - keto esters , 40 a , ß - Unsaturated aldehydes ...
... containing bonds , 33 conjugated double containing the styryl rest , 33 , 121-123 Unsaturated alcohols , from 1,3 - di- ketones , 24 from a - hydroxymethylene ketones , 24 , 25 from B - keto esters , 40 a , ß - Unsaturated aldehydes ...
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