The synthesis of unsymmetrically N-substituted chiral 1,4,7-triazacyclononanes
A number of chiral unsymmetrically N-substituted 1,4,7-triazacyclononane ligands have been prepared by modular methods. The key step in the synthesis centres on the macrocyclisation of three tertiary amide precursors under standard Richman-Atkins conditions which allows for subsequent N-functionalis...
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Veröffentlicht in: | Organic & biomolecular chemistry 2004-09, Vol.2 (18), p.2664-2670 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | A number of chiral unsymmetrically N-substituted 1,4,7-triazacyclononane ligands have been prepared by modular methods. The key step in the synthesis centres on the macrocyclisation of three tertiary amide precursors under standard Richman-Atkins conditions which allows for subsequent N-functionalisation. |
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ISSN: | 1477-0520 1477-0539 |
DOI: | 10.1039/b409259g |