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New oxime derivs. of macrolide antibiotic S541

机译:新的肟衍生。大环内酯类抗生素S541的研制

摘要

Macrotide antibiotic S541 oxime derivs. of formula (I) and their salts are new; where R1=methyl, ethyl or isopropyl; R2=H, 1-8C alkyl or 3-8C alkenyl, the groupNOR2 being in the E-configuration; an OR3=OH or substd. hydroxy group contg. upto 25 C-atoms. (I) may be prepd. by reaction of the corresponding oxo cpds. (II) with a reagent H2NOR2 or a salt thereof and, if desired, removing the portecting group from a resulting cpd.. (I) in which OR3 is a protected OH group. Cpds. (I) in which R2 is 1-8C alkyl or 3-8C alkenyl and OR3 is substd. hydroxy may be prepd. from corresponding cpds. in which OR3 is unsubstd. OH by reaction with a suitable O-substituting reagent.
机译:大环抗生素S541肟衍生。式(I)的化合物及其盐是新的;其中R1 =甲基,乙基或异丙基; R 2 = H,1-8C烷基或3-8C烯基,基团NOR 2为E-构型; OR3 = OH或substd。羟基续最多25个C原子。 (I)可以准备。通过相应的羰基cpds反应。 (II)用试剂H 2 NOR 2或其盐,并且,如果需要,从所得的cpd。(I)中除去连接基团。(I)其中OR 3是被保护的OH基。 Cpds。 (I),其中R 2是1-8C烷基或3-8C烯基且OR 3被取代。可以制备羟基。来自相应的cpds。其中OR3未被取代。通过与合适的O取代试剂反应生成OH。

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