Toda S, Nakagawa S, Naito T, Kawaguchi H
J Antibiot (Tokyo). 1980 Feb;33(2):173-81. doi: 10.7164/antibiotics.33.173.
Analogs of Bu-2313 A and B were prepared by C-acylation of tetramic acid derivatives with the dienoic acid moiety obtained by periodate oxidation of Bu-2313 A or B. The C-acylation proceeded in the presence of a strong base such as potassium t-butoxide, sodium hydride or lithium hydride, whereas the use of triethylamine afforded O-acylated products. The semi-synthetic Bu-2313 analogs exhibited antibacterial spectra similar to the parent antibiotic but none exceeded Bu-2313 B in activity.
通过用高碘酸盐氧化Bu - 2313 A或B得到的二烯酸部分对四胺酸衍生物进行C - 酰化反应,制备了Bu - 2313 A和B的类似物。C - 酰化反应在强碱如叔丁醇钾、氢化钠或氢化锂存在下进行,而使用三乙胺则得到O - 酰化产物。半合成的Bu - 2313类似物表现出与母体抗生素相似的抗菌谱,但在活性方面均未超过Bu - 2313 B。