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Glycine complex, polymer-based

Wulff and his collaborators reported, in 1989, the preparation of imprinted polymers able to perform enantioselective synthesis [11, 12]. The imprinting complex was prepared by reacting 3,4-di-hydroxy-phenyl-alanine methyl-ester (l-DOPA methyl ester) (16) with the 4-vinyl-salicylaldehyde (17) to form the corresponding Schiff s base (18), which was further reacted with the 4-vinyl-phenyl-boronic acid (19) to afford to the corresponding ester (20) (Scheme 4). The imprinting complex obtained was then polymerised and the template removed. The resulting polymers were incubated with sodium glycinate to allow formation... [Pg.312]


See other pages where Glycine complex, polymer-based is mentioned: [Pg.858]    [Pg.1135]    [Pg.858]    [Pg.292]    [Pg.7003]    [Pg.223]    [Pg.647]    [Pg.160]    [Pg.2661]    [Pg.331]    [Pg.160]   


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