Journal of Medicinal Chemistry p. 1577 - 1582 (1983)
Update date:2022-08-05
Topics: Synthesis IR spectroscopy Spectrophotometry Minimum inhibitory concentration (MIC) Substituent Effects Structure-Activity Relationship (SAR) Alkaline Hydrolysis Cephem Hydrolysis kinetics Chromatography (HPLC/TLC) β-Lactam Ring
Narisada, Masayuki
Yoshida, Tadashi
Ohtani, Mitsuaki
Ezumi, Kiyoshi
Takasuka, Mamoru
Relationships between intrinsic antibacterial activity and β-lactam reactivity of 7β-<(4-hydroxyphenyl)acetyl>amino- and 7β-<(4-hydroxyphenyl)malonyl>amino derivatives of 1-oxa- and 1-thiacephems, with or without the 7α-methoxy group (1-8), were investiga
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