The 2′-phenyl cinchonidine thiourea-catalyzed asymmetric addition of alcohols to isatin-derived N-Boc ketimines
-
Add time:07/13/2019 Source:sciencedirect.com
Optically active isatin-derived N,O-aminals were obtained through the catalytic asymmetric addition of various alcohols to isatin-derived N-Boc ketimines. Using 2′-phenyl cinchonidine thiourea as the catalyst, adducts were obtained in 96% yield and with up to 92% ee.
We also recommend Trading Suppliers and Manufacturers of BOC-(S)-3-AMINO-4-(3-TRIFLUOROMETHYL-PHENYL)-BUTYRIC ACID (cas 270065-77-5). Pls Click Website Link as below: cas 270065-77-5 suppliers
Prev:Catalytic asymmetric addition of arylboronic acids to N-Boc imines generated in situ using C2-symmetric cationic N-heterocyclic carbenes (NHCs) Pd2+ diaquo complexes
Next:Performance of cellulose acetate-ferric oxide nanocomposite supported metal catalysts toward the reduction of environmental pollutants) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Catalytic asymmetric addition of arylboronic acids to N-Boc imines generated in situ using C2-symmetric cationic N-heterocyclic carbenes (NHCs) Pd2+ diaquo complexes07/12/2019
- Synthesis of α,α-difluoro-β-hydroxy ketone via the La(OTf)3-catalyzed aldol reaction of carbonyl compounds with difluoroenol O-Boc esters07/11/2019
-
Health and Chemical more >


