Regioselectivity in Aromatic Claisen Rearrangements
✍ Scribed by Gozzo, Fábio Cesar; Fernandes, Sergio Antonio; Rodrigues, Denise Cristina; Eberlin, Marcos Nogueira; Marsaioli, Anita Jocelyne
- Book ID
- 120337868
- Publisher
- American Chemical Society
- Year
- 2003
- Tongue
- English
- Weight
- 145 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The (L-velopment of a highly enantioselective ~omatic Claisen remmlgement was achieved by the reaction of catechol mono allylic ethers with chiral boron reagent 1. This system was also shown to avoid the formation of para rearmagement and abnormal Claisen remrangement products.
Enantioselective Aromatic Claisen Rearrangement. -Allylic aromatic ethers bearing an (E)-or (Z)-side chain undergo highly enantioselective Claisen rearrangements in the presence of the chiral boron reagent (Ia). The method also avoids the formation of para or abnormal Claisen rearrangement products