| 摘要 |
<p>Oleandromycinoximes of common formula (I), where R1 = H, CH3, R2 = CH3, H or R1 and R2 = epoxy group, = CH2, R3 = OH, line ~ = single or double bond are prepared in a reaction of oleandromycine derivatives of common formula (II) with from 4- to 6- molar residual of hydroxylaminehydrochloride in presence of pyridine residual in nitrogen current in the room temperature during 2-40 hours. Consequently, the product is isolated. The above-described method of common formula (I) compounds preparation is significant for processing of the anti-microbial agents.</p> |
