An improvement for the synthesis of clarithromycin

Jian Hua Liang*, Guo Wei Yao

*此作品的通讯作者

科研成果: 期刊稿件文章同行评审

2 引用 (Scopus)

摘要

2′,4″-O-bis(trimethylsilyl)erythromycin A 9-0-(1- ethoxycyclohexyl)oxime was prepared for the regioselective methylation by using 1-ethoxycyclohexene as etherification agents and 1,1,1,3,3,3- hexamethyldisilazane as silylation reagents. Four successive reactions from erythromycin A oxime to clarithromycin were operated in the form of one-pot protection (including etherification and silylation), regioselective methylation and one-pot deprotection with overall yield 49.5%.

源语言英语
页(从-至)438-441
页数4
期刊Chinese Journal of Organic Chemistry
25
4
出版状态已出版 - 4月 2005

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