Enantioselective desymmetrization of meso-aziridines with aromatic thiols catalyzed by chiral bifunctional quaternary phosphonium salts derived from α-amino acids
-
Add time:08/25/2019 Source:sciencedirect.com
Desymmetrization of meso-aziridines with aromatic thiols was realized by using α-amino acids-derived chiral quaternary phosphonium salts catalysts to provide chiral β-amino sulfides with high yields (up to 99%) and in moderate enantioselectivities (up to 70%).
We also recommend Trading Suppliers and Manufacturers of 1-(p-Nitrobenzoyl)aziridine (cas 19614-29-0). Pls Click Website Link as below: cas 19614-29-0 suppliers
Prev:1.01 - Aziridines and Azirines: Monocyclic
Next:Synthesis of quinazolinone-based aziridine diols as chiral ligands: dual stereoselectivity in the asymmetric ethylation of aryl aldehydes) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Enantioselective desymmetrization of meso-N-(heteroarenesulfonyl)aziridines with TMSN3 catalyzed by chiral Lewis acids08/30/2019
- Chemistry of Carbohydrate Aziridines08/29/2019
- The stereochemistry of aziridine borane lithiation: diastereoselectivity and enantioselectivity08/28/2019
- 1.02 - Aziridines and Azirines: Fused-ring Derivatives08/27/2019
- Synthesis of quinazolinone-based aziridine diols as chiral ligands: dual stereoselectivity in the asymmetric ethylation of aryl aldehydes08/26/2019
- 1.01 - Aziridines and Azirines: Monocyclic08/24/2019
