LiBassi G, Monguzzi R, Broggi R, Broccali G, Carpi C, Pifferi G
J Antibiot (Tokyo). 1977 May;30(5):376-82. doi: 10.7164/antibiotics.30.376.
A number of penicillins (2) have been synthesized from the alpha-hydrazinoarylacetic acids (4) via the activated chloride hydrochlorides (5) or via the mixed anhydride of the corresponding N2-benzyloxycarbonyl derivatives (6). The penicillins, 2b, e, j, show good activity against gram-positive and gram-negative bacteria and enhanced penicillinase resistance in comparison with ampicillin.
已经通过活性氯化氢(5)或相应的N2 - 苄氧羰基衍生物的混合酸酐(6),由α-肼基芳基乙酸(4)合成了多种青霉素(2)。青霉素2b、2e、2j对革兰氏阳性菌和革兰氏阴性菌显示出良好的活性,并且与氨苄青霉素相比,对青霉素酶的抗性增强。