School of Chemistry, Trinity College Dublin, Trinity Biomedical Sciences Insitute, 152-160 Pearse Street, Dublin 2, Ireland.
Org Lett. 2013 Feb 1;15(3):504-7. doi: 10.1021/ol303310u. Epub 2013 Jan 18.
The use of intramolecular thiyl radical cyclizations for the synthesis of thiosugars has been investigated, and a new free-radical-based methodology for the synthesis of biologically important thiosugars has been developed. The methodology is mild and proceeds via either 6-endo or 5-exo cyclization to furnish the thiosugar ring. This represents the first examples of thiyl radical cyclization being applied to the synthesis of thiosugars.
人们研究了利用分子内硫自由基环化反应来合成硫代糖,由此开发出一种用于合成具有重要生物学意义的硫代糖的新自由基方法。该方法温和,通过 6-endo 或 5-exo 环化反应进行,生成硫代糖环。这代表了硫自由基环化反应首次应用于硫代糖的合成。