Posebna izdanja (Srpdka kraljevska akademija), Том 237 |
Из књиге
Резултати 1-3 од 42
Страница 20
... Addition of hydrogen derived from the hydrolyzing agent at 7 - position of ( XIX ) would give the enolic form of ( XXI ) , addition at the 9 - position would yield perinaph- thenol , and addition at any of the other possible positions ...
... Addition of hydrogen derived from the hydrolyzing agent at 7 - position of ( XIX ) would give the enolic form of ( XXI ) , addition at the 9 - position would yield perinaph- thenol , and addition at any of the other possible positions ...
Страница 32
... addition procedure at low temperatures ( -5o to 0o ) and by using a 1 : 2 molar ratio of hydride to acid.1545 CF ... addition ) while any unreacted acid is present . When the formation of ( VII ) has been completed , the addition of more ...
... addition procedure at low temperatures ( -5o to 0o ) and by using a 1 : 2 molar ratio of hydride to acid.1545 CF ... addition ) while any unreacted acid is present . When the formation of ( VII ) has been completed , the addition of more ...
Страница 183
... addition of to carbon dioxide with subsequent reduction , 31 addition of to nitriles , 86 analogy with lithium hydride , 2 , 102 aluminum Guanidino group , stability of , 99 Halides , 7 , 8 of indium and gallium , 8 see also Organic ...
... addition of to carbon dioxide with subsequent reduction , 31 addition of to nitriles , 86 analogy with lithium hydride , 2 , 102 aluminum Guanidino group , stability of , 99 Halides , 7 , 8 of indium and gallium , 8 see also Organic ...
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