Posebna izdanja (Srpdka kraljevska akademija), Том 237 |
Из књиге
Резултати 1-3 од 10
Страница 68
... linkage undergo mainly rupture of the primary linkage , forming secondary and tertiary alcohols , respectively , 3 , 144 , 86 , 326 , 688 , 689 , 695 , 697 , 698 , 1358 , 1369 , 1512 , 1648 whereas catalytic hydrogenation in the ...
... linkage undergo mainly rupture of the primary linkage , forming secondary and tertiary alcohols , respectively , 3 , 144 , 86 , 326 , 688 , 689 , 695 , 697 , 698 , 1358 , 1369 , 1512 , 1648 whereas catalytic hydrogenation in the ...
Страница 85
... linkage , producing benzaldehyde ( XIII ) and a - phenyl - y - diethylaminopropionitrile ( XIV ) , 907 ( CH ) 2N - CH - CH - C - C - CH C6H5 CHSCHO + NC O XII XIII C6H5 ( C2HN - CH2CH2 - CH - CN XIV The reduction of B ...
... linkage , producing benzaldehyde ( XIII ) and a - phenyl - y - diethylaminopropionitrile ( XIV ) , 907 ( CH ) 2N - CH - CH - C - C - CH C6H5 CHSCHO + NC O XII XIII C6H5 ( C2HN - CH2CH2 - CH - CN XIV The reduction of B ...
Страница 125
... linkage in the a , B - position to the carboxyl , carbonyl or ester group undergoes partial reduction to the double ... linkage is reactive and may be converted by partial reduction to an ethylenic linkage , 850-855 , 1424 , 1692 , 1707 ...
... linkage in the a , B - position to the carboxyl , carbonyl or ester group undergoes partial reduction to the double ... linkage is reactive and may be converted by partial reduction to an ethylenic linkage , 850-855 , 1424 , 1692 , 1707 ...
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