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Arylamides, lithium

Wen and Grutzner used, among other NMR parameters, the QSC of the lithium enolate of acetaldehyde to deduce that it exists as tetramers of different solvation in THF and THF/n-hexane solvent systems . However, the most thorough study of Li QSC and the most interesting in the present context was reported by Jackman and coworkers in 1987167 -pjjg effects on the QSC values of both aggregation and solvation in a number of organolithium systems was studied in this paper, i.e. different arylamides, phenolates, enolates, substituted phenyllithium complexes and lithium phenylacetylide. [Pg.164]

The Li QSC values may be correlated with the effects of structure, solvent and temperature on association in solution for arylamides such as lithium indolide (249) and lithium A-alkylanilides (250a-c). ... [Pg.375]

See other pages where Arylamides, lithium is mentioned: [Pg.164]    [Pg.129]    [Pg.60]    [Pg.207]    [Pg.162]    [Pg.164]    [Pg.129]    [Pg.60]    [Pg.207]    [Pg.162]    [Pg.165]    [Pg.81]    [Pg.197]   
See also in sourсe #XX -- [ Pg.129 ]



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