Reaction of monensin silver salt with methyl iodide: smooth alkylation of a tightly hydrogen-bonded carboxylate

被引：0

作者：

Inagaki, Yoshio ^{[1
]}

Shishido, Tadao ^{[1
]}

机构：

[1] Fujifilm Corp, Synthet Organ Chem Labs, Kaisei, Kanagawa 2588577, Japan

来源：

SUPRAMOLECULAR CHEMISTRY | 2011年 / 23卷 / 1-2期

关键词：

monensin; ionophore; ion selective electrode; esterification; intramolecular hydrogen bond; POLYETHER ANTIBIOTIC MONENSIN; ION-SELECTIVE ELECTRODE; CHEMICAL-MODIFICATION; SODIUM-ION; MOLECULAR-STRUCTURE; BIOLOGICAL-ACTIVITY; TRANSPORT ACTIVITY; CRYSTAL-STRUCTURE; METAL-IONS; COMPLEXES;

D O I：

10.1080/10610278.2010.506550

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Despite its structural similarity to the sparingly reactive sodium salt of monensin, the silver salt of monensin was smoothly alkylated with methyl iodide on the carboxyl group to give the methyl ester of monensin.

引用

页码：19 / 21

页数：3

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