Subat, Michael and Koenig, Burkhard (2001) N-arylation of 1,4,7,10-tetraazacyclododecanes. SYNTHESIS-STUTTGART (12). pp. 1818-1825. ISSN 0039-7881
Full text not available from this repository. (Request a copy)Abstract
Palladium-catalyzed N-arylation reactions provide acces to N-aryl-substituted and N-aryl-bridged 1,4,7,10-tetracazacy-cyclododecanes. Yields of arylation products are low with simple haloarenes, whereas reactions with pyridine derivatives give substituted cyclens in moderate to satisfactory yields.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | PALLADIUM-CATALYZED AMINATION; CROSS-COUPLING REACTIONS; AZA-CROWN ETHERS; MACROCYCLIC TETRAAMINE; SELECTIVE RECOGNITION; COPPER(II) COMPLEXES; AQUEOUS-SOLUTION; ARYL CHLORIDES; BOND FORMATION; METAL-IONS; azamacrocycle; palladium; N-arylation |
| Subjects: | 500 Science > 540 Chemistry & allied sciences |
| Divisions: | Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Burkhard König |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 13 Dec 2021 17:03 |
| Last Modified: | 13 Dec 2021 17:03 |
| URI: | https://pred.uni-regensburg.de/id/eprint/41177 |
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