A thioxanone-based [2,3]-sigmatropic rearrangement strategy which delivers Cβ-chiral pent-4-enoic acids with excellent Cβ-induction is reported.
|Original language||English (US)|
|Number of pages||3|
|Journal||Journal of Organic Chemistry|
|State||Published - 1990|
ASJC Scopus subject areas
- Organic Chemistry
Kurth, M. J., Tahir, S. H., & Olmstead, M. M. (1990). A thioxanone-based chiral template: Asymmetric induction in the [2,3]-sigmatropic rearrangement of sulfur ylids. Enantioselective preparation of Cβ-chiral pent-4-enoic acids. Journal of Organic Chemistry, 55(8), 2286-2288.