本文概述了胺硝基物选择氧化还原羰基化生成脲的新工艺路线。
The third chapter was devoted to the study of quantitative structure-activity relationship(QSAR) for indazolyl ureas as TRPV1 antagonists.第三章致力于吲唑脲类辣椒素受体(TRPV1)通道拮抗剂的定量构效关系(QSAR)研究。
By retrieving concerned Literatures, this article discussed comprehensively the biological activities of phenyl ureas, acyl ureas and tetrazoles.本文通过检索文献,对苯脲类、酰基脲类、酰基硫脲类及四唑类化合物的生物活性作了系统的论述。