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 |
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页(从-至) | 438-441 |
页数 | 4 |
期刊 | Chinese Journal of Organic Chemistry |
卷 | 25 |
期 | 4 |
出版状态 | 已出版 - 4月 2005 |