Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering , Tokyo Medical and Dental University (TMDU) , 2-3-10 Kanda-Surugadai , Chiyoda-ku, Tokyo 101-0062 , Japan.
Org Lett. 2019 Jul 5;21(13):5252-5258. doi: 10.1021/acs.orglett.9b01862. Epub 2019 Jun 25.
The synthetic utility of 3-thioaryne intermediates has been demonstrated through an aryne relay approach. The efficient synthesis of o-silylaryl triflate-type 3-thioaryne precursors has been achieved by the regioselective silylthiolation of 3-(triflyloxy)arynes with silyl sulfides. Various 3-thioarynes were successfully generated from these precursors and reacted with various arynophiles to afford diverse multisubstituted aryl sulfides. Further derivatizations of the products enabled easy access to the novel sulfur-containing π-extended heterocycles, which demonstrates the utility of this method.
通过芳炔重氮中间体方法,证明了 3-硫芳炔中间体的合成实用性。通过硅基硫醚的区域选择性硅基硫代芳炔与 3-(三氟甲磺酰氧基)芳炔反应,有效地合成了邻位硅基芳基三氟甲磺酸酯型 3-硫芳炔前体。从这些前体中成功生成了各种 3-硫芳炔,并与各种芳炔试剂反应,得到了各种多取代芳基硫醚。产物的进一步衍生化使得容易获得新型含硫的π扩展杂环,这证明了该方法的实用性。