Enantioselective β-Replacement Reaction Mediated by an Artificial Enzyme Composed of a Hydrophobia Vitamin B6, Chiral Bilayer-forming Lipids, and Copper(II) Ions
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/22/4/22_4_645/_pdf
Reference4 articles.
1. Functionalized Bilayer Membranes as Artificial Tryptophan Synthase. Characterization of Catalytic Efficiency, Substrate Specificity, and Reaction Selectivity
2. Preparation of stable single-compartment vesicles with cationic and zwitterionic amphiphiles involving amino acid residues
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1. Development of Unprotected Syntheses in Aqueous Media;YAKUGAKU ZASSHI;2013-02-01
2. Convenient synthesis of chiral tryptophan derivatives using Negishi cross-coupling;Tetrahedron;2011-08
3. Mechanism for the direct synthesis of tryptophan from indole and serine: a useful NMR technique for the detection of a reactive intermediate in the reaction mixture;Magnetic Resonance in Chemistry;2010-08-27
4. ChemInform Abstract: Enantioselective β-Replacement Reaction Mediated by an Artificial Enzyme Composed of a Hydrophobic Vitamin B6, Chiral Bilayer-Forming Lipids, and Copper(II) Ions.;ChemInform;2010-08-19
5. Bifunctional Binols: Chiral 3,3′‐Bis(aminomethyl)‐1,1′‐bi‐2‐naphthols (Binolams) in Asymmetric Catalysis;European Journal of Organic Chemistry;2009-05
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