Assignment of the absolute configuration to winterstein's acid, R-3-dimethylamino-3-phenyl propionic acid, by the asymmetric synthesis of homochiral (S)-(+)-ethyl 3-dimetylamino-3-phenyl propionate-Science-Chemical Encyclopedia-lookchem

Assignment of the absolute configuration to winterstein's acid, R-3-dimethylamino-3-phenyl propionic acid, by the asymmetric synthesis of homochiral (S)-(+)-ethyl 3-dimetylamino-3-phenyl propionate
Add time:07/24/2019 Source:sciencedirect.com

The asymmetric synthesis of homochiral (S)-(+)-ethyl 3-dimethylamino-3-phenyl propionate, via stereoselective Michael addition of lithium dimethylamide to (S)-Z-[(η5-C5H5)-Fe(CO)(PPh3)COCHCHPh] and oxidative decomplexation, establishes the absolute configuration of Winterstein's acid, 3-dimethylamino-3-phenyl propionic acid, derived from Taxine B, as R.

We also recommend Trading Suppliers and Manufacturers of 3-(9-Anthryl)propionic Acid Ethyl Ester (cas 109690-74-6). Pls Click Website Link as below: cas 109690-74-6 suppliers

Prev:Application of the modified 2-methoxy-2-(1-naphthyl)propionic (MαNP) acid method to steroidal alcohols and the most efficient HPLC separation found in diastereomeric MαNP esters
Next: Synthesis and use of α-aminophosphine oxides and N,N-bis(phosphinoylmethyl)amines – A study on the related ring platinum complexes)

Click to view details

Encyclopedia