Brickner S J, Gaikema J J, Zurenko G E, Greenfield L J, Manninen P R, Ulanowicz D A
Upjohn Laboratories, Upjohn Company, Kalamazoo, Michigan 49001.
J Antibiot (Tokyo). 1992 Feb;45(2):213-26. doi: 10.7164/antibiotics.45.213.
The synthesis and antibacterial activity of a series of N-acyl 3-isopropylidenyl- and 3-isopropyl 2-azetidinones having potent in vitro antibacterial activity, particularly against anaerobic organisms, is described. A distinguishing structural feature of these compounds is the lack of any ionizable moiety appendant to the lactam nitrogen.
描述了一系列具有强大体外抗菌活性,特别是对厌氧生物有活性的N-酰基-3-异亚丙基-和3-异丙基-2-氮杂环丁酮的合成及其抗菌活性。这些化合物的一个显著结构特征是在内酰胺氮上没有任何可离子化的附属部分。