Posebna izdanja (Srpdka kraljevska akademija), Том 237 |
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Страница v
... reagents of universal application . Lithium aluminum hydride , however , is undoubtedly such a reagent . It has already proved itself so useful that it has become indispensable and even unique in chemical laboratories . To all research ...
... reagents of universal application . Lithium aluminum hydride , however , is undoubtedly such a reagent . It has already proved itself so useful that it has become indispensable and even unique in chemical laboratories . To all research ...
Страница 2
... reagents . The similarity between the two compounds is also shown by the fact that the Grignard reagent may be successfully replaced by lithium aluminum hydride for the determination of active hydrogen in organic compounds ( see IV ) ...
... reagents . The similarity between the two compounds is also shown by the fact that the Grignard reagent may be successfully replaced by lithium aluminum hydride for the determination of active hydrogen in organic compounds ( see IV ) ...
Страница 13
... reagent ** in an- hydrous ether , and by separating the undissolved residue either by sedimentation or filtration . The clear solution may be stored in a specially but simply devised apparatus , which also permits the con- venient ...
... reagent ** in an- hydrous ether , and by separating the undissolved residue either by sedimentation or filtration . The clear solution may be stored in a specially but simply devised apparatus , which also permits the con- venient ...
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