Nilov, Dmitry and Raecker, Reinhard and Reiser, Oliver (2002) Synthesis of 1,4-oxazepin-7-ones using Baylis-Hillman products as key intermediates. SYNTHESIS-STUTTGART (15). pp. 2232-2242. ISSN 0039-7881, 1437-210X
Full text not available from this repository. (Request a copy)Abstract
Baylis-Hilman adducts derived from aromatic aldehydes and methyl acrylate can be readily converted to 1,4-oxazepin-7- ones substituted in 2-, 3-, or 4-position by condensation with amino alcohols.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | DIELS-ALDER REACTIONS; 2-PYRIDYL DERIVATIVES; THERMAL CYCLIZATION; INDOLIZINES; ALKALOIDS; Baylis-Hillman reaction; 1,4-oxazepin-7-ones; amino alcohols; aromatic aldehydes; lactonization; hydrogenation |
| Subjects: | 500 Science > 540 Chemistry & allied sciences |
| Divisions: | Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Oliver Reiser |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 25 Aug 2021 12:34 |
| Last Modified: | 25 Aug 2021 12:34 |
| URI: | https://pred.uni-regensburg.de/id/eprint/39762 |
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