Posebna izdanja (Srpdka kraljevska akademija), Том 237 |
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Страница 90
... AROMATIC NITRO COMPOUNDS The reduction of aromatic nitro compounds produces azo com- pounds , 3 , 188 , 953 , 957 , 961 which are resistant , under normal conditions , to further reduction ( however , see XX , 1 ) . 2ArNo2 + 2LIAIHA Ar ...
... AROMATIC NITRO COMPOUNDS The reduction of aromatic nitro compounds produces azo com- pounds , 3 , 188 , 953 , 957 , 961 which are resistant , under normal conditions , to further reduction ( however , see XX , 1 ) . 2ArNo2 + 2LIAIHA Ar ...
Страница 128
... AROMATIC HYDROCARBONS Unsubstituted aromatic hydrocarbons are in general very stable toward lithium aluminum hydride , and can be partially reduced only under very drastic experimental conditions . Phenanthrene is not changed even when ...
... AROMATIC HYDROCARBONS Unsubstituted aromatic hydrocarbons are in general very stable toward lithium aluminum hydride , and can be partially reduced only under very drastic experimental conditions . Phenanthrene is not changed even when ...
Страница 178
... Aromatic acids , 29 esters of , 34 , 35 Aromatic halides , 104 Aromatic nitro compounds , 90 color reaction of , 90 detection of , 90 Aromatic nitro esters , selective re- duction of , 90 Aromatic systems , 128-132 partial reduction of ...
... Aromatic acids , 29 esters of , 34 , 35 Aromatic halides , 104 Aromatic nitro compounds , 90 color reaction of , 90 detection of , 90 Aromatic nitro esters , selective re- duction of , 90 Aromatic systems , 128-132 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