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Updated: Jun 10, 2026

Enzymatic Cascade Reactions for the Synthesis of Chiral Amino Alcohols from L-lysine
Published on: February 16, 2018
Heterogeneous chiral copper complexes of amino alcohol for asymmetric nitroaldol reaction
Vishal J Mayani1, Sayed H R Abdi, Rukhsana I Kureshy
1Discipline of Inorganic Materials & Catalysis, Central Salt and Marine Chemicals Research Institute, Council of Scientific & Industrial Research, Bhavnagar-364 002, Gujarat, India.
Abstract:
Chiral amino alcohols supported on mesoporous silicas were synthesized and evaluated as a new class of chiral ligands in copper-catalyzed nitroaldol reaction under heterogeneous and mild reaction conditions. The activity and enantioselectivity of the present catalytic system is immensely influenced by the presence of achiral and chiral bases as an additive. The heterogenized chiral copper(II) complex of amino alcohol was found to be an effective recyclable catalyst for the nitroaldol reaction of different aldehydes such as aromatic, aliphatic, alicyclic, and α-β unsaturated aldehydes to produce nitroaldol products with remarkably high enantioselectivity (≥99%) and yields.
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