Posebna izdanja (Srpdka kraljevska akademija), Том 237 |
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Страница 36
... HALOGEN ESTERS Halogen esters are reduced selectively , under usual conditions , to halogen alcohols , 302 , 357 , 358 , 366 , 426 , 454 , 475 , 487 , 494 , 511 , 539 , 549 , 607 , 906 , 949 , 1183 , 1192 , 1194 , 1198 , 1207 , 1227 ...
... HALOGEN ESTERS Halogen esters are reduced selectively , under usual conditions , to halogen alcohols , 302 , 357 , 358 , 366 , 426 , 454 , 475 , 487 , 494 , 511 , 539 , 549 , 607 , 906 , 949 , 1183 , 1192 , 1194 , 1198 , 1207 , 1227 ...
Страница 103
... halogen atoms , 86 , 808 , 809 , 1691 and of compounds containing , besides the halogen function , other reducible groups , * such as halogen ketones and halogen aldehydes , 90 , 93 , 98 , 100 , 108 , 111 , 251 , 252 , 1010 , 1060 ...
... halogen atoms , 86 , 808 , 809 , 1691 and of compounds containing , besides the halogen function , other reducible groups , * such as halogen ketones and halogen aldehydes , 90 , 93 , 98 , 100 , 108 , 111 , 251 , 252 , 1010 , 1060 ...
Страница 183
... Halogen , 105 allyl - type activated , 36 , attached to unsaturated carbon at- hydro- oms , 105 synthesis of , Ethyl ... Halogen acid chlorides , 45 , 103 Halogen acids , 32 , 103 Halogen alcohols , formation of , 16 , 17 , 32 , 36 , 39 ...
... Halogen , 105 allyl - type activated , 36 , attached to unsaturated carbon at- hydro- oms , 105 synthesis of , Ethyl ... Halogen acid chlorides , 45 , 103 Halogen acids , 32 , 103 Halogen alcohols , formation of , 16 , 17 , 32 , 36 , 39 ...
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