| Literature DB >> 25250516 |
Matthias Leiendecker1, Chien-Chi Hsiao, Lin Guo, Nurtalya Alandini, Magnus Rueping.
Abstract
The direct replacement of aromatic methoxy groups with activated carbon nucleophiles would give rise to novel synthetic pathways for targeted and diversity-oriented syntheses. We demonstrate here that this transformation can be achieved in a one-step reaction involving a bifunctional organolithium nucleophile in combination with a CAr OMe bond-cleaving nickel catalyst. The resulting products are stable, α-CH active, and suitable for various further modifications.Entities:
Keywords: CO bond cleavage; aryl ethers; cross-coupling; methoxy functionalization; nickel
Year: 2014 PMID: 25250516 DOI: 10.1002/anie.201402922
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336