Enantioselective Henry reaction catalyzed by a novel L-(+)-aspartic acid-derived Schiff base ligand and Cu (II) ion
Mild and efficient enantioselective Henry reactions of nitromethane with various aldehydes
were catalyzed by a novel L-(+)-aspartic acid-derived Schiff base ligand in the presence of
Cu (II) ions, affording the corresponding adducts in high yields (up to 96%) and
enantioselectivities (up to 92% ee).
were catalyzed by a novel L-(+)-aspartic acid-derived Schiff base ligand in the presence of
Cu (II) ions, affording the corresponding adducts in high yields (up to 96%) and
enantioselectivities (up to 92% ee).
Abstract
Mild and efficient enantioselective Henry reactions of nitromethane with various aldehydes were catalyzed by a novel L-(+)-aspartic acid-derived Schiff base ligand in the presence of Cu (II) ions, affording the corresponding adducts in high yields (up to 96%) and enantioselectivities (up to 92% ee).
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