Bohlmann–Rahtz pyridine synthesis
Source: Wikipedia, the free encyclopedia.
| Bohlmann–Rahtz pyridine synthesis | |
|---|---|
| Named after | Ferdinand Bohlmann Dieter Rahtz |
| Reaction type | Ring forming reaction |
| Identifiers | |
| Organic Chemistry Portal | bohlmann-rahtz-pyridine-synthesis |
In
pyridines in two steps, first a condensation reaction between an enamine and an ethynylketone to form an aminodiene intermediate, which after heat-induced E/Z isomerization undergoes a cyclodehydration to yield 2,3,6-trisubstituted pyridines.[1][2][3][4]
References
 | This chemical reaction article is a stub. You can help Wikipedia by expanding it. |