From Nitrobenzenes to Substituted 1,2,3,4-Tetrahydroquinolines in a Single Step by a Domino Reduction/Imine Formation/Aza-Diels – Alder Reaction
- Publikations-Art
- Zeitschriftenbeitrag (peer-reviewed)
- Autoren
- Imrich, H.-G.; Conrad, J.; Bubrin, D; Beifuss, U.
- Erscheinungsjahr
- 2015
- Veröffentlicht in
- J. Org. Chem.
- Band/Volume
- 80/
- DOI
- 10.1021/jo502882y
- Seite (von - bis)
- 2319-2332
The three-component reaction between a nitrobenzene, an aldehyde, and a dienophile in the presence of iron powder as a reductant and montmorillonite K10 as a catalyst in aqueous citric acid delivers the products of an aza-Diels–Alder (Povarov) reaction with high endo-selectivity and yields up to 99%.