Medimagh Raouf, Marque Sylvain, Prim Damien, Chatti Saber, Zarrouk Hédi
Institut Lavoisier de Versailles (ILV) UMR CNRS 8180, Université de Versailles-Saint-Quentin-en-Yvelines, 45 Avenue des Etats-Unis, 78 035 Versailles, Cedex, France.
J Org Chem. 2008 Mar 21;73(6):2191-7. doi: 10.1021/jo7024916. Epub 2008 Feb 27.
Selective metal-free amination and Diels-Alder reactions are described in the furan series, leading to polysubstituted anilines or to stable oxabicyclic adducts in high yield. Interestingly, anilines are conveniently prepared through a novel one-pot, two-step amination/Diels-Alder procedure from commercially available 5-bromo-2-furaldehyde.
在呋喃系列中描述了选择性无金属胺化反应和狄尔斯-阿尔德反应,可高产率地生成多取代苯胺或稳定的氧杂双环加合物。有趣的是,通过一种新颖的一锅两步胺化/狄尔斯-阿尔德方法,由市售的5-溴-2-糠醛可方便地制备苯胺。