Asymmetric syntheses of (S)-α-amino acids in 28--98% optical yields via double chiral induction in alkylations of ketimine 1 derived from (+)-2-hydroxypinan-3-one and (-)-men- thyl glycinate which is a chiral match p...Asymmetric syntheses of (S)-α-amino acids in 28--98% optical yields via double chiral induction in alkylations of ketimine 1 derived from (+)-2-hydroxypinan-3-one and (-)-men- thyl glycinate which is a chiral match pair have been studied. The factors controlling the diastereoselec- tivities in alkylation reactions of the ketimine, the properties of alkylating agents and various alkylation conditions are examined.展开更多
基金the National Natural Science Foundation of China.
文摘Asymmetric syntheses of (S)-α-amino acids in 28--98% optical yields via double chiral induction in alkylations of ketimine 1 derived from (+)-2-hydroxypinan-3-one and (-)-men- thyl glycinate which is a chiral match pair have been studied. The factors controlling the diastereoselec- tivities in alkylation reactions of the ketimine, the properties of alkylating agents and various alkylation conditions are examined.
