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Organometallic reagents and strong bases

In some cases, however, the use of ethyllithium-diethyl ether-LiSr is to be [Pg.9]

In contrast to alkylations with most of the alkyl halides, the reactions of anions with ethylene oxide in organic solvents such as diethyl ether and THE [Pg.10]

Alkyllithium bases are generally less suitable for deprotofiation of compounds with strongly electron-withdrawing groups such as C=0, COOR and CsN. In these cases lithium dialkylamides, especially those with bulky groups (isopropyl, cyclohexyl), are the reagents of choice. They are very easily obtained from butyllithium and the dialkylamine in the desired solvent. [Pg.10]


See other pages where Organometallic reagents and strong bases is mentioned: [Pg.9]    [Pg.145]    [Pg.152]   


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