Posebna izdanja (Srpdka kraljevska akademija), Том 237 |
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Страница 37
... methyl group . Ethyl 3 - indolecarboxylate undergoes hydro- genolysis even under ordinary conditions of operation1426 ( see XV , 1 ; XVI , 1 ) . The 3 - ethoxycarbonyl group in pyrrole is likewise reduced to a methyl group , 187 and ...
... methyl group . Ethyl 3 - indolecarboxylate undergoes hydro- genolysis even under ordinary conditions of operation1426 ( see XV , 1 ; XVI , 1 ) . The 3 - ethoxycarbonyl group in pyrrole is likewise reduced to a methyl group , 187 and ...
Страница 63
... methyl - 1 , 2 , 3 , 4 - tetrahydro- quinazoline ( along with a small amount of 3 - methyl - 3,4 - dihydro- quinazoline ) , or partially to the 1,2 - dihydro - 3 - methyl - 4 ( 3H ) -quinazo- linone , 1645 When reduced with lithium ...
... methyl - 1 , 2 , 3 , 4 - tetrahydro- quinazoline ( along with a small amount of 3 - methyl - 3,4 - dihydro- quinazoline ) , or partially to the 1,2 - dihydro - 3 - methyl - 4 ( 3H ) -quinazo- linone , 1645 When reduced with lithium ...
Страница 187
... Methyl cyclopropyl ketone , 16 N - Methyldioxindoles , 63 Methyl 4,6 - ditosyl - 2,3 - anhydro - a- D - alloside , of , 114 selective reductions 3,4 - Methylenedioxy - 5 - bromo - ẞ - ni- trostyrene , 104 Methyl ethyl ketone ...
... Methyl cyclopropyl ketone , 16 N - Methyldioxindoles , 63 Methyl 4,6 - ditosyl - 2,3 - anhydro - a- D - alloside , of , 114 selective reductions 3,4 - Methylenedioxy - 5 - bromo - ẞ - ni- trostyrene , 104 Methyl ethyl ketone ...
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