Abstract
Vinylindoles and vinylpyrroles were prepared from their corresponding aldehydes or ketones using the Peterson olefination, or by use of the Nysted reagent, a commercially available gem-dimetallic compound. The two methods provide efficient and convenient access to these useful heterocyclic 1,3-diene systems.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 381-388 |
| Number of pages | 8 |
| Journal | Journal of Heterocyclic Chemistry |
| Volume | 48 |
| Issue number | 2 |
| DOIs | |
| State | Published - Mar 2011 |
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