Posebna izdanja (Srpdka kraljevska akademija), Том 237 |
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Страница 28
... attack by lithium aluminum hydride from the rear face with the hydride hydrogen entering the a - configu ration , 267 , 269 , 258 , 1510 which is a direct consequence of the steric arrangement of the polycyclic system , can also be ...
... attack by lithium aluminum hydride from the rear face with the hydride hydrogen entering the a - configu ration , 267 , 269 , 258 , 1510 which is a direct consequence of the steric arrangement of the polycyclic system , can also be ...
Страница 55
... attack by lithium aluminum hydride . 423 , 424 , 611 , 1010 , 1257 Quinone imides ( ortho and para ) , with a calculated quantity of lithium aluminum hydride , are exclusively converted to diamides.635 2. REARRANGEMENT REACTIONS AND ...
... attack by lithium aluminum hydride . 423 , 424 , 611 , 1010 , 1257 Quinone imides ( ortho and para ) , with a calculated quantity of lithium aluminum hydride , are exclusively converted to diamides.635 2. REARRANGEMENT REACTIONS AND ...
Страница 61
... attack by lithium aluminum hydride , probably as a result of the steric arrangement of the ring which is of such nature as to shield one oxo group by the neighboring aryl or alkyl substituents.1636 3 - Phenyl - 3- ( B ...
... attack by lithium aluminum hydride , probably as a result of the steric arrangement of the ring which is of such nature as to shield one oxo group by the neighboring aryl or alkyl substituents.1636 3 - Phenyl - 3- ( B ...
Садржај
LITHIUM ALUMINUM HYDRIDE AS A REDUCING AGENT IN | 1 |
III | 7 |
Special Procedures and Preparation of Hydride Solutions | 13 |
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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