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机构地区:[1]河南职工医学院,河南郑州450003 [2]河南大学药学院,河南开封475001
出 处:《中国医药工业杂志》2003年第2期65-66,共2页Chinese Journal of Pharmaceuticals
摘 要:S)-(+)-2-Amino-1-propanol, the key chiral intermediate of levofloxacin, was preparation from L-2-aminopropionic acid by methyl esterification, and then direct reduction by KBH 4 without purification with an overall yield of 70%.S)-(+)-2-Amino-1-propanol, the key chiral intermediate of levofloxacin, was preparation from L-2-aminopropionic acid by methyl esterification, and then direct reduction by KBH 4 without purification with an overall yield of 70%.
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