Bohlmann–Rahtz pyridine synthesis
Chemical reaction
From Wikipedia, the free encyclopedia
In organic chemistry, the Bohlmann–Rahtz pyridine synthesis is a reaction that generates substituted 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]
| Bohlmann–Rahtz pyridine synthesis | |
|---|---|
| Named after | Ferdinand Bohlmann Dieter Rahtz |
| Reaction type | Ring forming reaction |
| Identifiers | |
| Organic Chemistry Portal | bohlmann-rahtz-pyridine-synthesis |
