Efficient synthesis of chiral 2,2'-bipyrrolidines by an anti-selective alkene diamination.

@article{Mller2012EfficientSO,
  title={Efficient synthesis of chiral 2,2'-bipyrrolidines by an anti-selective alkene diamination.},
  author={Christian H. M{\"u}ller and Roland Fr{\"o}hlich and Constantin G Daniliuc and Ulrich Hennecke},
  journal={Organic letters},
  year={2012},
  volume={14 23},
  pages={5944-7}
}
The rapid and efficient construction of complex chiral bicyclic amines is possible using a novel alkene diamination reaction. Electrophilic iodinating agents promote the intramolecular anti-selective diamination of alkenes and allow the efficient synthesis of chiral amines such as trans-bipyrrolidines. 
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