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

Amino Acids

Volumn 43, Issue 1, 2012, Pages 299-308

  Belokon, Yuri N ^a   Gugkaeva, Zalina T ^a   Hakobyan, Karine V ^b   Maleev, Victor I ^a   Moskalenko, Margarita A ^a   Khrustalev, Victor N ^a   Saghyan, Ashot S ^b   Tsaloev, Alan T ^a   Babievsky, Kiryl K ^a  

^a A N NESMEYANOV INSTITUTE OF ORGANOELEMENT COMPOUNDS   (Russian Federation)

^b YEREVAN STATE UNIVERSITY   (Armenia)

Author keywords

Carboxyglutamic acid; Asymmetric organocatalysis; Glutamic acid; Michael addition

Indexed keywords

3,3' BIS(HYDROXYDIPHENYLMETHYL)[1,1' BIPHTHALENE] 2,2' DIOL; 4 CARBOXYGLUTAMIC ACID DERIVATIVE; DEHYDROALANINE SCHIFF BASE NICKEL COMPLEX; GLUTAMIC ACID DERIVATIVE; GLYCINE; NICKEL COMPLEX; SCHIFF BASE; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; CONTROLLED STUDY; CRYSTAL STRUCTURE; ENANTIOMER; ORGANOCATALYST; PRIORITY JOURNAL; STRUCTURE ACTIVITY RELATION; SYNTHESIS;

1-CARBOXYGLUTAMIC ACID; ALANINE; CATALYSIS; GLUTAMIC ACID; GLYCINE; NAPHTHOLS; NICKEL; SCHIFF BASES; STEREOISOMERISM;

EID: 84862773314     PISSN: 09394451     EISSN: 14382199     Source Type: Journal    
DOI: 10.1007/s00726-011-1076-y     Document Type: Article

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