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Using the same organocatalyst for asymmetric synthesis of both enantiomers of glutamic acid-derived Ni(II) complexes via 1,4-additions of achiral glycine and dehydroalanine Schiff base Ni(II) complexes
Authors:Yuri N. Belokon  Zalina T. Gugkaeva  Karine V. Hakobyan  Victor I. Maleev  Margarita A. Moskalenko  Victor N. Khrustalev  Ashot S. Saghyan  Alan T. Tsaloev  Kiryl K. Babievsky
Affiliation:Institute of Russian Academy of Sciences, A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Vavilov str. 28, 119991, Moscow, Russia. yubel@ineos.ac.ru
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.
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