Laboratoire de Physicochimie des Matériaux et des Biomolécules, EA 4244, Faculté des Sciences et Techniques de Tours, Parc de Grandmont, 37200 Tours, France.
J Org Chem. 2011 Oct 21;76(20):8347-54. doi: 10.1021/jo201528u. Epub 2011 Sep 15.
In the presence of copper(I) iodide, heteroaromatic β-iodo-α,β-unsaturated carboxylic acid systems opposed to terminal alkyne afford selectively 6-endo-dig cyclization products via a tandem coupling oxacyclization reaction.
在碘化亚铜存在的情况下,杂芳基β-碘代-α,β-不饱和羧酸体系与末端炔烃反应,通过串联偶联环氧化反应选择性地生成 6-endo-dig 环化产物。