Abstract
[GRAPHICS]
A new strategy for the asymmetric synthesis of chiral primary alpha-ferrocenylalkylamines has been utilized to generate homochiral redox-active receptors that bind chiral carboxylate anions with moderate enantioselectivity and undergo a redox response to complexation.
Original language | English |
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Volume | 4 |
DOIs | |
Publication status | Published - 14 Nov 2002 |
Keywords
- ORGANOMETALLIC REAGENTS
- ENANTIOSELECTIVE SYNTHESIS
- MOLECULAR RECOGNITION
- ORGANOLITHIUM COMPOUNDS
- OXIME ETHERS
- AMINO-ACIDS
- 1,2-ADDITION
- 1-FERROCENYLALKYLAMINES
- DERIVATIVES
- THIOUREA