Expedient Route to the Functionalized Calyciphylline A-Type Skeleton via a Michael Addition–RCM Strategy
An efficient, robust, and scalable strategy to access the functionalized core of calyciphylline A-type alkaloids has been developed starting from commercially available 3-methylanisole. Key features of this approach are an intramolecular Michael addition/allylation sequence and a ring-closing metathesis step.
Références
- Titre
- Expedient Route to the Functionalized Calyciphylline A-Type Skeleton via a Michael Addition–RCM Strategy
- Type de publication
- Article de revue
- Année de publication
- 2011
- Auteurs
- Sladojevich, Filippo, Michaelides Iacovos N., Darses Benjamin, Ward John W., and Dixon Darren J.
- Revue
- Organic Letters
- Volume
- 13
- Pagination
- 5132–5135
Soumis le 25 septembre 2018