Schmaderer, Harald and Hohenleutner, Andreas and Koenig, Burkhard (2009) Synthesis of a Bicyclic Diamine Derived from Kemp's Acid. SYNTHETIC COMMUNICATIONS, 39 (14): PII 912469. pp. 2596-2604. ISSN 0039-7911, 1532-2432
Full text not available from this repository. (Request a copy)Abstract
A bicyclic diamine with defined and stable conformation in solution was prepared from Kemp's triacid. The efficient four-step synthesis of the Boc-protected diamine requires only a single purification by column chromatography. X-ray analysis and NMR spectroscopy confirm the structure of the diamine in the solid state and in solution.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | CONVERGENT FUNCTIONAL-GROUPS; ENANTIOSELECTIVE PROTONATION; CHIRAL IMIDES; AMIDE; Diamine; Kemp's triacid; piperidine |
| 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: | 14 Oct 2020 06:02 |
| Last Modified: | 14 Oct 2020 06:02 |
| URI: | https://pred.uni-regensburg.de/id/eprint/29893 |
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