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Amino Acids ; 43(1): 299-308, 2012 Jul.
Article in English | MEDLINE | ID: mdl-21935708

ABSTRACT

(S)- and (R)-BIMBOL were efficient PT catalysts of asymmetric Michael addition of prochiral Ni-PBP-Gly (1) to acrylic esters and malonic esters to Ni-PBP-Δ-Ala (2) correspondingly. The salient feature of the catalysis is opposite configurations of Glu prepared via the two paths with BIMBOL of the same configuration and a perspective novel catalytic procedure for the synthesis of Gla derivatives.


Subject(s)
Glutamic Acid/chemistry , Naphthols/chemistry , Schiff Bases/chemistry , 1-Carboxyglutamic Acid/chemistry , Alanine/analogs & derivatives , Alanine/chemistry , Catalysis , Glycine/chemistry , Naphthols/metabolism , Nickel/chemistry , Stereoisomerism
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