A new convenient transformation of erythromycin A into clarithromycin

被引:9
作者
Allevi, P [1 ]
Longo, A [1 ]
Anastasia, M [1 ]
机构
[1] Univ Milan, Dipartimento Chim & Biochem Med, I-20133 Milan, Italy
关键词
antibiotics; antibacterials; clarithromycin; erythromycin A; methylation;
D O I
10.1016/S0968-0896(99)00230-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Erythromycin A was transformed into clarithromycin by the sequence of reactions: selective thexyldimethylsilylation of the 9-oxime, trimethylsilylation of the 2',4 "-hydroxy groups, methylation of the resulting 2',4 "-[O-bis(trimethylsilyl)]-9-[O-(dimethylthexylsilyl)oxime] and acidic regeneration of the protected functionalities. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2749 / 2752
页数:4
相关论文
共 12 条
[11]   CHEMICAL MODIFICATION OF ERYTHROMYCINS .11. SYNTHESIS OF CLARITHROMYCIN (6-O-METHYLERYTHROMYCIN A) VIA ERYTHROMYCIN A QUATERNARY AMMONIUM SALT DERIVATIVE [J].
WATANABE, Y ;
KASHIMURA, M ;
ASAKA, T ;
ADACHI, T ;
MORIMOTO, S .
HETEROCYCLES, 1993, 36 (02) :243-247
[12]  
1997, Patent No. 9736912