Abstract
Copper(II) complexes based on two diastereopure camphor-derived iminomethylpyridine ligands were resolved and structurally characterised by single-crystal X-ray diffraction. Each chiral Cu(II) complex was an efficient catalyst for theenantioselective Henry reaction of phenyl propionaldehyde and nitromethane, affording 1-nitro-4-phenylbutan-2-ol in high yields (up to 99%) and excellent enantioselectivities (up to 99%) that were governed by the combined chirality effect of the ligand backbone and side-chain.
Original language | English |
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Article number | 109880 |
Journal | Inorganic Chemistry Communications |
Volume | 144 |
DOIs | |
State | Published - Oct 2022 |
Keywords
- Camphor-derived iminomethylpyridines
- Chiral-copper(II) complex
- Diastereopure
- Enantioselective Henry reaction
- Resolution