Posebna izdanja (Srpdka kraljevska akademija), Том 237 |
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Резултати 1-3 од 15
Страница 24
... diol.230 The keto form ( XLI ) in aliphatic and alicyclic 1,3 - diketones showing tautomerism * is normally reduced to the diol ( XLIII ) , while the enol tautomer ( XLII ) reacts with the hydride with elimination of an oxygen atom ...
... diol.230 The keto form ( XLI ) in aliphatic and alicyclic 1,3 - diketones showing tautomerism * is normally reduced to the diol ( XLIII ) , while the enol tautomer ( XLII ) reacts with the hydride with elimination of an oxygen atom ...
Страница 72
... diol diacetate , 1510 17a , 203 - epoxyallopregnane - 38,20a - diol diacetate , 1654 and other sub- stituted epoxides.144 On the other hand it was found , by studying the effect of electronic factors on the direction of ring opening of ...
... diol diacetate , 1510 17a , 203 - epoxyallopregnane - 38,20a - diol diacetate , 1654 and other sub- stituted epoxides.144 On the other hand it was found , by studying the effect of electronic factors on the direction of ring opening of ...
Страница 182
... diol , 126 Diphenyliodonium bromide , 105 . Diphenyl mercury , 7 · a , ẞ- Diphenyl- ẞ methoxyacrilonitrile , 84 , 85 ... diol diacetate , 72 3,4 - Epoxy - 1 - butene , 73 1a - 2a - Epoxy - 3 - cholestanone , 27 a , f ...
... diol , 126 Diphenyliodonium bromide , 105 . Diphenyl mercury , 7 · a , ẞ- Diphenyl- ẞ methoxyacrilonitrile , 84 , 85 ... diol diacetate , 72 3,4 - Epoxy - 1 - butene , 73 1a - 2a - Epoxy - 3 - cholestanone , 27 a , f ...
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