Charest Mark G, Lerner Christian D, Brubaker Jason D, Siegel Dionicio R, Myers Andrew G
Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA 02138, USA.
Science. 2005 Apr 15;308(5720):395-8. doi: 10.1126/science.1109755.
Complex antibiotics based on natural products are almost invariably prepared by semisynthesis, or chemical transformation of the isolated natural products. This approach greatly limits the range of accessible structures that might be studied as new antibiotic candidates. Here we report a short and enantioselective synthetic route to a diverse range of 6-deoxytetracycline antibiotics. The common feature of this class is a scaffold of four linearly fused rings, labeled A through D. We targeted not a single compound but a group of structures with the D ring as a site of structural variability. A late-stage, diastereoselective C-ring construction was used to couple structurally varied D-ring precursors with an AB precursor containing much of the essential functionality for binding to the bacterial ribosome. Five derivatives were synthesized from benzoic acid in yields ranging from 5 to 7% over 14 to 15 steps, and a sixth, (-)-doxycycline, was synthesized in 8.3% yield over 18 steps.
基于天然产物的复杂抗生素几乎都是通过半合成或对分离出的天然产物进行化学转化来制备的。这种方法极大地限制了可能作为新抗生素候选物进行研究的可及结构范围。在此,我们报道了一条简短且对映选择性的合成路线,可用于制备多种6-脱氧四环素类抗生素。这类抗生素的共同特征是由四个线性稠合环组成的骨架,标记为A至D。我们的目标不是单一化合物,而是以D环作为结构可变位点的一组结构。采用后期非对映选择性的C环构建方法,将结构多样的D环前体与含有与细菌核糖体结合所需大部分关键官能团的AB前体偶联。从苯甲酸出发,经过14至15步反应合成了五种衍生物,产率在5%至7%之间,另外,经过18步反应合成了第六种衍生物(-)-多西环素,产率为8.3%。