Abstract
A delicate interplay of several kinetically labile ligands is required for reactions that proceed through serial ligand catalysis mechanisms. An investigation of the disruption of this balance has enabled the development of a method for the intermolecular allylic C-H alkylation of unactivated as well as activated α-olefins (see example, Bn=benzyl).
| Original language | English (US) |
|---|---|
| Pages (from-to) | 6824-6827 |
| Number of pages | 4 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 50 |
| Issue number | 30 |
| DOIs | |
| State | Published - Jul 18 2011 |
Keywords
- C-H activation
- allylic alkylation
- ligand effects
- palladium catalysis
- sulfoxide ligands
ASJC Scopus subject areas
- Catalysis
- General Chemistry