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Deprotonation with aluminum amides

Finally, a chiral triamine 35, derived from (-)-proline, has been used as the lithium salt for the deprotonation of amines (Section D.2.I.). It is obtained from A-benzyloxycarbonylproline by forming the amide with, .Ar,A -trimethyl-l,2-ethanediamine, cleavage of the protecting group, and lithium aluminum hydride reduction29. [Pg.14]


See other pages where Deprotonation with aluminum amides is mentioned: [Pg.210]    [Pg.210]    [Pg.143]    [Pg.95]    [Pg.377]    [Pg.214]    [Pg.621]    [Pg.391]    [Pg.193]    [Pg.219]   
See also in sourсe #XX -- [ Pg.210 ]




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