Posebna izdanja (Srpdka kraljevska akademija), Том 237 |
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Страница 113
... sulfinic acids ( or their further reduction products ) and phenols ( equation b ) . 832 , 678 , 820 , 834 , 839 Thus , for example , l - menthyl p - toluenesulfonate was reduced to trans- p - menthane , 832 , 6 and phenyl p ...
... sulfinic acids ( or their further reduction products ) and phenols ( equation b ) . 832 , 678 , 820 , 834 , 839 Thus , for example , l - menthyl p - toluenesulfonate was reduced to trans- p - menthane , 832 , 6 and phenyl p ...
Страница 118
... SULFINIC AND SULFENIC ACIDS Sulfonyl chlorides ( RSO2CI ) are converted by means of lithium aluminum hydride to sulfinic acids , disulfides or mercaptans ( thio- phenols ) , the result of the reduction depending on the ratio of re ...
... SULFINIC AND SULFENIC ACIDS Sulfonyl chlorides ( RSO2CI ) are converted by means of lithium aluminum hydride to sulfinic acids , disulfides or mercaptans ( thio- phenols ) , the result of the reduction depending on the ratio of re ...
Страница 191
... acids showing , 29 , 30 , 33 , 45 disulfides showing , 110 disulfonates showing , 115 effect of on ɑ - amino ... Sulfinic acids , 118 Sulfinyl chlorides , 118 Sulfite esters , 119 Sulfonamides , 118 Sulfones , 111 Sulfonic esters , 112 ...
... acids showing , 29 , 30 , 33 , 45 disulfides showing , 110 disulfonates showing , 115 effect of on ɑ - amino ... Sulfinic acids , 118 Sulfinyl chlorides , 118 Sulfite esters , 119 Sulfonamides , 118 Sulfones , 111 Sulfonic esters , 112 ...
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