综述了近年来恶唑烷酮类和喹诺酮类抗菌药物的研究进展。
This paper reviews advances in the research of the antibacterials of oxazolidinones and quinolones.
本文是关于新型抗菌剂恶唑烷酮类化合物的设计、合成及其抗菌活性的研究。
The design, synthesis and antibacterial activity of new oxazolidinone derivatives was studied in this paper.
Joseph Pernerstorfer： 取代的恶唑烷酮和其在血液凝固领域中的应用。
Substituted oxazolidinones and their use in the field of blood coagulation.
目的用电子束辐照技术去除水溶液中的呋喃唑酮的代谢产物3 -氨基- 2 -恶唑烷酮(简称aoz)。
Objective: To remove the furazolidone metabolite 3-amino-2-oxazolidinone (AOZ) from water medium by electronic irradiation.
这些反应在质子性醇溶剂与K_2CO_3组成的两相体系中进行更为方便，可用于吡咯烷及恶唑烷衍生物的合成。
The reactions are performed more conveniently in two phase systems consisted of alcoholic solvents and K_2CO_3, and may be adapted for the synthesis of pyrrolidine and oxazolidine derivatives.
因此，本论文主要在超临界二氧化碳中进行了以下两部分工作：一是利用二氧化碳合成环状碳酸酯；二是利用二氧化碳合成恶唑烷酮。
Hence, two parts of researches were carried out under supercritical carbon dioxide in this paper, including the synthesis of cyclic carbonates and the synthesis of oxazolidinones.
因此，本论文主要在超临界二氧化碳中进行了以下两部分工作：一是利用二氧化碳合成环状碳酸酯；二是利用二氧化碳合成恶唑烷酮。
Hence, two parts of researches were carried out under supercritical carbon dioxide in this paper, including the synthesis of cyclic carbonates and the synthesis of oxazolidinones.
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