Abstract
Catalytic enantioselective conjugate additions of simple alkyl groups to nitroalkenes or cyclic enones that result in the formation of tertiary C–C bonds are described. For these stereoselective addition reactions, new chiral phosphino-oxazoline ligands were synthesized and used. The reactions were promoted by a Cu-based catalyst (2 mol-%), and gave the chiral products in up to 92 % yield with 95 % ee. A larger-scale synthesis was demonstrated, and the origin of the stereoselectivity was proposed based on DFT calculations.
| Original language | English |
|---|---|
| Pages (from-to) | 3122-3130 |
| Number of pages | 9 |
| Journal | European Journal of Organic Chemistry |
| Volume | 2018 |
| Issue number | 24 |
| DOIs | |
| State | Published - 29 Jun 2018 |
Bibliographical note
Publisher Copyright:© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Keywords
- Asymmetric catalysis
- Ligand design
- Michael addition
- N,P ligands
- Nucleophilic addition
- Zinc