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An efficient chiral synthesis of (R)-N-[3-acetyl-4-(2-hydroxy-3-isopropylamino-propoxy)phenyl]-butanamide with high enantioselectivity

An efficient chiral synthesis of (R)-N-[3-acetyl-4-(2-hydroxy-3-isopropylamino-propoxy)phenyl]-butanamide with high enantioselectivity
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摘要 R-Enantiomer of the β-receptor antagonist N-[3-acetyl-4-(2-hydroxy-3-isopropylamino-propoxy)phenyl] butanamide with high enantioselectivity was synthesized from cheap starting materials and enantiopure chiral reagent through an efficient,convenient and practical synthetic strategy.Title product was detected by 1H NMR,13C NMR,and MS,and the enatiomeric excess was determined by chiral HPLC analysis using a chiracel AD-H column. R-Enantiomer of the β-receptor antagonist N-[3-acetyl-4-(2-hydroxy-3-isopropylamino-propoxy)phenyl] butanamide with high enantioselectivity was synthesized from cheap starting materials and enantiopure chiral reagent through an efficient, convenient and practical synthetic strategy. Title product was detected by 1H NMR, 13C NMR, and MS, and the enatiomeric excess was determined by chiral HPLC analysis using a chiracel AD-H column.
出处 《Science China Chemistry》 SCIE EI CAS 2009年第8期1216-1219,共4页 中国科学(化学英文版)
基金 Supported by the National Natural Science Foundation of China (Grant Nos. 20472090 & 10576034) PLA General Armament Department (Grant No. 9140A28010707zk7301)
关键词 CHIRAL synthesis ENANTIOSELECTIVITY enatiomeric excess CHIRAL HPLC analysis chiral synthesis enantioselectivity enatiomeric excess chiral HPLC analysis
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参考文献23

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