Additive Pummerer rearrangements. Asymmetric synthesis of (–)-methyl jasmonate
- 1 January 1985
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 9,p. 542-543
- https://doi.org/10.1039/c39850000542
Abstract
Examples of mild, additive Pummerer rearrangements are given; one example involves asymmetric carbon–carbon bond formation as the key step for synthesis of (–)-methyl jasmonate.Keywords
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