研究了一种简单而温和的合成芴醇的方法，可以选择性地获得9溴芴（9 BF）。
A simple and mild method for the synthesis of fluorenol was studied and 9 bromofluorene (9 BF) can be selectively obtained.
目的探讨本芴醇衍生物LY980 5 0 3对肿瘤多药耐药的逆转作用及其作用机理。
AIM To investigate the reversing effect of LY980503 (a benflumetol derivative) on multidrug resistance of MCF/Dox cell line and its mechanism.
结果提示抗青琥酯恶性疟原虫对苯芴醇无交叉抗性，青蒿琥酯与苯芴醇伍用在体外测定中具有一定增效作用；
The results suggested that the resistant isolates of P. falciparum have sign of crossing resistance to artemether and dihydroarteannuin, but have no cross-resistance to benflumetolum.
方法采用双盲随机对比法，共收治恶性疟患者151例，其中蒿甲醚为50例，本芴醇为51例，复方蒿甲醚为50例。
Methods Of 151 patients, 50 patients were treated with artemether , 51 patients were treated with benflumetol and 50 patients were treated with combined regime(co-artemether).
研究了芴与N 溴代丁二酰亚胺（NBS）的光化学反应及其溴代产物的水解反应，提供了一种温和、简便的制备芴醇的方法。
A simple and mild method for the synthesis of fluorenol was studied. 9 bromofluorene (9 BF) can be selectively obtained by the photochemical reaction of fluorene with N bromosuccinimide (NBS).
研究了芴与N 溴代丁二酰亚胺（NBS）的光化学反应及其溴代产物的水解反应，提供了一种温和、简便的制备芴醇的方法。
A simple and mild method for the synthesis of fluorenol was studied. 9 bromofluorene (9 BF) can be selectively obtained by the photochemical reaction of fluorene with N bromosuccinimide (NBS).
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