摘要
利用氯霉素中间体对硝基苯基丝氨酸甲酯为原料,合成了具有分支杆菌生长素部分结构的2,4,5-三取代噁唑啉化合物27个。经初步药理筛选,活性均不显著。
From threo-3-(4-nitrophenyl)serine methyl ester, twenty seven
of 2-oxazolines with 2,4,5-substitutions have been synthesized. None of them had
significant antituberculotic activity by preliminary tests.
出处
《中国医药工业杂志》
CAS
CSCD
北大核心
1989年第5期197-200,共4页
Chinese Journal of Pharmaceuticals
