Abstract
2-Metallo-2-sulfonylpropanes and 2-metallo-2-nitropropanes react with the dimethyl alkylidenemalonate derived from the acetonide of D- glyceraldehyde to produce the Michael adduct or the corresponding dimethyl cyclopropane-1,1-dicarboxylate. The nature of the product formed and the relative configuration of the cyclopropane derivative depends upon the nature of the leaving group and the conditions used (solvent and counter ion).
| Original language | English |
|---|---|
| Pages (from-to) | 1936-1938 |
| Number of pages | 3 |
| Journal | Synlett |
| Issue number | 12 |
| Publication status | Published - 1 Jan 1999 |