Posebna izdanja (Srpdka kraljevska akademija), Том 237 |
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Страница 30
... acid can be converted to its ester 127 , 302 , 333 , 1552 or acid chloride ( see IX ) , which are in general easily reduced to alcohols . Optically active carboxylic acids give optically pure alcohols without racemization of the ...
... acid can be converted to its ester 127 , 302 , 333 , 1552 or acid chloride ( see IX ) , which are in general easily reduced to alcohols . Optically active carboxylic acids give optically pure alcohols without racemization of the ...
Страница 32
Srpska akademija nauka i umetnosti. 3. HALOGEN ACIDS Halogen acids react without loss of the halogen atoms producing ... acid 326 and 5 - bromo- and 2,5 - dichloro - 3 - thenoic acids , 1544 which were readily con- verted to the halogen ...
Srpska akademija nauka i umetnosti. 3. HALOGEN ACIDS Halogen acids react without loss of the halogen atoms producing ... acid 326 and 5 - bromo- and 2,5 - dichloro - 3 - thenoic acids , 1544 which were readily con- verted to the halogen ...
Страница 33
Srpska akademija nauka i umetnosti. 4. DICARBOXYLIC ACIDS Dicarboxylic acids are readily reduced to diols , 139 , 297 ... acid , 365 and 3 - chlorophthalic acid which could not be reduced beyond the lactone stage . 366 In most cases the ...
Srpska akademija nauka i umetnosti. 4. DICARBOXYLIC ACIDS Dicarboxylic acids are readily reduced to diols , 139 , 297 ... acid , 365 and 3 - chlorophthalic acid which could not be reduced beyond the lactone stage . 366 In most cases the ...
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