Harrar, Klaus and Reiser, Oliver (2012) Enantioselective synthesis of (-)- paeonilide. CHEMICAL COMMUNICATIONS, 48 (28). pp. 3457-3459. ISSN 1359-7345,
Full text not available from this repository. (Request a copy)Abstract
The first enantioselective synthesis of (-)- paeonilide is reported. Starting from inexpensive furan-3-carboxylic acid the targeted monoterpene was obtained in 12 steps via an asymmetric cyclopropanation-lactonization cascade and a stereoselective side chain insertion at an acetal-like position.
Item Type: | Article |
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Uncontrolled Keywords: | STEREOSELECTIVE-SYNTHESIS; CARBENE INSERTION; (+/-)-PAEONILIDE; DERIVATIVES; CATALYSTS; FURANS; |
Divisions: | Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Oliver Reiser |
Depositing User: | Dr. Gernot Deinzer |
Date Deposited: | 25 May 2020 07:16 |
Last Modified: | 25 May 2020 07:16 |
URI: | https://pred.uni-regensburg.de/id/eprint/19531 |
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