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naphthylglycyl and tetrahydronaphthylglycyl - cephalosporin antibiotics and procedure for its manufacture

机译:萘基甘氨酰和四氢萘基甘氨酰-头孢菌素类抗生素及其制备方法

摘要

PROCEDURE FOR THE OBTAINING OF CEPHALOSPORINS AND THEIR PHYSIOLOGICALLY COMPATIBLE SALTS, OF FORMULA (I), IN WHICH A AND B ARE HYDROGEN OR TOGETHER FORM A DOUBLE LINK; R1-R6 MAY BE SEVERAL TYPES OF RADICALS, CONSISTING IN THE REACTION OF CLARIFICATION OF A COMPOUND OF FORMULA (II) WITH A CLARIFYING AGENT OF FORMULA (III), OR AN ACTIVE DERIVATIVE OF THE SAME, IN WHICH ALL THE SYMBOLS HAVE THE SAME MEANING THAT IN THE FORMULA (I). THE ACILATION IS CARRIED OUT IN A COMMON ORGANIC SOLVENT, INERT, IN THE PRESENCE OF A BASE, AT A TEMPERATURE INCLUDING BETWEEN C20ºC AND 60ºC. THESE COMPOUNDS HAVE PHARMACOLOGICAL APPLICATIONS FOR THE TREATMENT OF BACTERIAL DISEASES. (Machine-translation by Google Translate, not legally binding)
机译:在甲和乙为氢或双链形式的情况下获得头孢菌素及其生理相容性盐的程序(一); R1-R6可能是几种自由基,其形式为澄清化合物(II)与澄清剂(III)的反应,或该化合物的活性衍生物,同时所有符号都相同公式中的含义(I)。在碱存在下,在20°C至60°C的温度下,通过普通的有机溶剂(惰性)进行酸化。这些化合物在治疗细菌性疾病中具有药理学应用。 (通过Google翻译进行机器翻译,没有法律约束力)

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