Department of Translational Molecular Pathology, M. D. Anderson Cancer Center, The University of Texas Houston, TX USA.
Front Chem. 2014 Aug 1;2:55. doi: 10.3389/fchem.2014.00055. eCollection 2014.
Synthesis of a new methoxy dibenzofluorene through alkylation, cyclodehydration and aromatization in a one-pot operation is achieved for the first time. Using this hydrocarbon, a few derivatives are prepared through aromatic nitration, catalytic hydrogenation, coupling reaction with a side chain and reduction. The benzylic position of this hydrocarbon with the side chain is oxidized and reduced. Some of these derivatives have demonstrated excellent antitumor activities in vitro. This study confirms antitumor activity depends on the structures of the molecules.
首次通过一锅法实现了通过烷基化、环脱水和芳构化合成新的甲氧基二苯并芴。使用这种碳氢化合物,通过芳香硝化、催化氢化、与侧链偶联反应和还原制备了几种衍生物。该带有侧链的碳氢化合物的苄位被氧化和还原。这些衍生物中的一些在体外表现出优异的抗肿瘤活性。该研究证实抗肿瘤活性取决于分子的结构。