Cycloadditions of 3-methoxyfuran with mono-activated dienophiles; application to the synthesis of (±)-avenaciolides
- 1 January 1981
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 5,p. 221-222
- https://doi.org/10.1039/c39810000221
Abstract
Cycloadditions of 3-methoxyfuran (1) with several mono-activated dienophiles gave the endo adducts stereoselectively under the usual conditions in satisfactory yields; two of the adducts were transformed into potential intermediates (7a) and (7b) for the synthesis of (±)-avenaciolide and (±)-isoavenaciolide, respectively.Keywords
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