详细研究了氟代苯基硼酸和多芳基硼酸的合成及其工艺改进。
The synthesis of fluoro-substituted phenylboronic acid, and multiarylboronic acid and their process improvement were studied in detail.
目的研究多芳基取代蝶啶类化合物的合成及其抗肿瘤活性。
Aim To study the synthesis and antitumour activities of some aryl-substituted pteridines.
本研究对一种新的多芳基取代咪唑化合物fg020327的体外逆转活性及其逆转机制进行了探讨。
This study was to explore MDR reversal activity of a novel compound FG020327, and its mechanism.
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