Institute of Organic Chemistry , University of Vienna , Währinger Strasse 38 , 1090 Vienna , Austria.
CeMM Research Center for Molecular Medicine , Austrian Academy of Sciences , Lazarettgasse 14, AKH BT 25.3 , 1090 Vienna , Austria.
J Am Chem Soc. 2019 Sep 4;141(35):13772-13777. doi: 10.1021/jacs.9b07185. Epub 2019 Aug 22.
FR252921, FR252922, and FR256523 are a family of potent macrocyclic polyene immunosuppressive agents with a novel mode of action. However, the lack of an efficient and flexible synthesis has hindered further biological studies, mostly due to the fact that the natural products appear to be kinetic isomers regarding the triene moiety. Herein, we report the development and application of an unprecedented, unique domino Suzuki-Miyaura/4π-electrocyclic ring-opening macrocyclization, resulting in a concise, unified, and stereoselective synthetic route to these complex targets in only 10 steps. This in turn enables ready access to a range of unnatural analogues, among which several compounds showed inhibition of T-lymphocyte proliferation at levels equal or superior to those of the natural products themselves.
FR252921、FR252922 和 FR256523 是一类具有新型作用模式的强效大环聚烯免疫抑制剂。然而,由于天然产物在三烯部分似乎是动力学异构体,缺乏高效灵活的合成方法阻碍了进一步的生物学研究。在此,我们报告了一种前所未有的独特的串联铃木-宫浦/4π-电环化开环大环化反应的开发和应用,该反应导致这些复杂靶标仅通过 10 步即可实现简洁、统一和立体选择性的合成路线。这反过来又可以方便地获得一系列非天然类似物,其中几种化合物在抑制 T 淋巴细胞增殖方面的水平与天然产物相当或更高。