Abstract
Furylpyridines, thienylpyridines, and imidazolylpyridines were obtained regioselectively in 40‐67% yields from the reaction of heteroaryllithiums with N‐ethoxycarbonylpyridinium chloride or N‐ethoxycarbonyl‐3‐methylpyridinium chloride in the presence of Cul in a catalytic amount at −78 °C or −50°C, then followed by oxidation. The regioselectivity of this reaction depended upon temperature of the reaction and the nature of heteroaryllithiurn.
| Original language | English |
|---|---|
| Pages (from-to) | 75-79 |
| Number of pages | 5 |
| Journal | Journal of the Chinese Chemical Society |
| Volume | 41 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - Feb 1994 |
| Externally published | Yes |
Keywords
- Furylpyridines
- Heteroarylpyridines
- Imidazylpyridines
- N‐Ethoxycarbonylpyridinium chloride
- Thienylpyridines
ASJC Scopus subject areas
- General Chemistry