Abstract
An efficient, green and atom-economical iron-catalyzed hydroamination of vinylpyridines with azoles has been developed. This reaction works smoothly for a diverse range of vinylpyridines and azoles, including diazoles and triazoles. The reaction was catalyzed by 5 mol % FeCl3 in toluene at 110 °C for 3 h to afford the anti-Markovnikov hydroamination products in moderate to excellent yields and excellent selectivities.
Original language | English (US) |
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Pages (from-to) | 694-697 |
Number of pages | 4 |
Journal | Asian Journal of Organic Chemistry |
Volume | 6 |
Issue number | 6 |
DOIs | |
State | Published - Jun 2017 |
Externally published | Yes |
Keywords
- anti-Markovnikov
- azoles
- hydroamination
- iron
- vinylpyridines
ASJC Scopus subject areas
- Organic Chemistry