期刊:Chemistry Letters [Oxford University Press] 日期:1978-11-01卷期号:7 (11): 1253-1256被引量:43
标识
DOI:10.1246/cl.1978.1253
摘要
Abstract An asymmetric synthesis of α-hydroxy aldehydes was achieved in high optical yields starting from a keto aminal, prepared from phenylglyoxal and (S)-2-(anilinomethyl)pyrrolidine. By treating the keto aminal with the Grignard reagents and the hydrolysis of resulting hydroxy aminals, α-hydroxy aldehydes were obtained in 94–95% optical yields.