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采用两种新选择性保护方法由L-丝氨酸和α-酮戊二酸为原料经几步合成了8个目标化合物。体外抑菌该验表明除TMV外,对金葡球菌209P和大肠杆菌44822具有中等到强的活性。
Two new selective protection methods were used to synthesize 8 target compounds from L-serine and α-ketoglutaric acid in several steps. In Vitro Antibacterial This test showed moderate to strong activity against Staphylococcus aureus 209P and E. coli 44822 in addition to TMV.