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- URN to cite this document:
- urn:nbn:de:bvb:355-epub-341981
- DOI to cite this document:
- 10.5283/epub.34198
Alternative links to fulltext:DOI
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.
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