Resolution of racemic amino acids via stereoselective ligand-exchange reactions on an optically pure nickel(II) complex
Racemic amino acids (Ala, Val, Leu) co-ordinate steroselectively to the square-planar chiral matrix complex [Ni{(S,S)-L)}]2+{(S,S)-L =N,N′-bis[(2S)-pyrrolidin-2-yl]propane-1,3-diamine}. The stereoselectivities [Ala, 60%(S), 40%(R); Val, 75%(S), 25%(R); Leu, 68%(S), 32%(R)] have been predicted by mol...
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| Hauptverfasser: | , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
1993
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| In: |
Dalton transactions
Year: 1993, Heft: 13, Pages: 2023-2026 |
| ISSN: | 1477-9234 |
| DOI: | 10.1039/DT9930002023 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1039/DT9930002023 Verlag, lizenzpflichtig, Volltext: https://pubs.rsc.org/en/content/articlelanding/1993/dt/dt9930002023 |
| Verfasserangaben: | Paul V. Bernhardt, Peter Comba, Trevor W. Hambley, Imre Sávágó, Katalin Várnagy |
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| 520 | |a Racemic amino acids (Ala, Val, Leu) co-ordinate steroselectively to the square-planar chiral matrix complex [Ni{(S,S)-L)}]2+{(S,S)-L =N,N′-bis[(2S)-pyrrolidin-2-yl]propane-1,3-diamine}. The stereoselectivities [Ala, 60%(S), 40%(R); Val, 75%(S), 25%(R); Leu, 68%(S), 32%(R)] have been predicted by molecular mechanics calculations and determined experimentally by potentiometric titrations. The structure of the chiral matrix complex has also been determined: orthorhombic, space group P212121, a= 8.298(3), b= 13.513(4), c= 18.293(7)Å, Z= 4, R′= 0.051. | ||
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| 700 | 1 | |a Sávágó, Imre |e VerfasserIn |4 aut | |
| 700 | 1 | |a Várnagy, Katalin |e VerfasserIn |4 aut | |
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