Cu (II)-catalyzed asymmetric henry reaction with a novel C1-symmetric aminopinane-derived ligand

A novel C1-symmetric dinitrogen ligand was synthesized in high yield from commercially available (1R,2R,3R,5S)-(-)-isopinocampheylamine and 1-methyl-2-imidazolecarboxaldehyde. In combination with Cu(OAc)2H2O, this new ligand promote the reaction between nitromethane and aliphatic aldehydes with high...

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Veröffentlicht in:Molecules (Basel, Switzerland) Switzerland), 2015-04, Vol.20 (4), p.6224-6236
Hauptverfasser: Filippova, Liudmila, Stenstrøm, Yngve, Hansen, Trond Vidar
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Sprache:eng
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Zusammenfassung:A novel C1-symmetric dinitrogen ligand was synthesized in high yield from commercially available (1R,2R,3R,5S)-(-)-isopinocampheylamine and 1-methyl-2-imidazolecarboxaldehyde. In combination with Cu(OAc)2H2O, this new ligand promote the reaction between nitromethane and aliphatic aldehydes with high yields (up to 97%) and moderate enantioselectivities (up to 67% ee). The reactions with benzaldehyde required prolonged reaction time that resulted in diminished yields, but accompanied with ee-values in the 55%-76% range.
ISSN:1420-3049
1420-3049
DOI:10.3390/molecules20046224