Laboratory for Advanced Materials & Institute of Fine Chemicals, East China University of Science and Technology, 130 Mei Long Road, Shanghai 200237, PR China.
Chemistry. 2012 Mar 19;18(12):3654-8. doi: 10.1002/chem.201103404. Epub 2012 Feb 22.
The addition of nucleophiles to C=N bonds offers a highly efficient synthetic strategy for accessing nitrogen-containing molecules.1 Among the well-developed addition reactions, such as the highly efficient Mannich reaction, various C-H bond-activated compounds including carboxylic acid derivatives, nitroalkanes, and terminal alkynes have been applied as nucleophiles to achieve different classes of amines.2 However, employing new nucleophiles without activated C-H bonds, such as internal alkynes and allenic esters are limited when using metal catalysts.3 Herein, we wish to report a new addition of allenic esters to C=N bonds initiated by a silver-catalyzed 1,3-migration of propargylic esters.
亲核试剂与 C=N 键的加成反应为构建含氮分子提供了一种高效的合成策略。1 在已发展成熟的加成反应中,如高效的曼尼希反应,各种 C-H 键活化化合物,包括羧酸衍生物、硝基烷烃和末端炔烃,已被用作亲核试剂,以实现不同类型的胺。2 然而,在使用金属催化剂时,采用没有活化 C-H 键的新亲核试剂,如内炔和烯丙基酯的应用受到限制。3 在此,我们希望报道一种新的含烯丙基酯的加成反应,该反应由银催化的丙炔酯的 1,3-迁移引发。