Abstract
(formula presented) Addition of electron-rich alkenes to the peroxycarbenium ions derived from Lewis acid-mediated ionization of 3-alkoxy-1,2-dioxolanes provides natural product related to the plakinic acids.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1391-1393 |
| Number of pages | 3 |
| Journal | Organic Letters |
| Volume | 1 |
| Issue number | 9 |
| DOIs | |
| State | Published - Nov 4 1999 |
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
Fingerprint Dive into the research topics of 'Lewis acid-mediated displacements of alkoxydioxolanes: Synthesis of a 1,2-dioxolane natural product'. Together they form a unique fingerprint.
Cite this
Dussault, P. H., & Liu, X. (1999). Lewis acid-mediated displacements of alkoxydioxolanes: Synthesis of a 1,2-dioxolane natural product. Organic Letters, 1(9), 1391-1393. https://doi.org/10.1021/ol990954y