Lee Sang-Hyeup, Yoshida Kazuhiro, Matsushita Hana, Clapham Bruce, Koch Guido, Zimmermann Jürg, Janda Kim D
Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
J Org Chem. 2004 Dec 10;69(25):8829-35. doi: 10.1021/jo048353u.
Primary ureas have been used as substrates in rhodium-catalyzed N-H insertion reactions with an array of diazocarbonyls. The insertion reaction is efficient and gives excellent selectivity and yields. The products from the insertion reaction with diazoketones cyclize readily in the presence of acid to yield the corresponding imidazolones that can be further derivatized by N-alkylation with alkyl, allyl, and benzyl halides. Alternatively, the imidazolones were treated with phosphorus oxybromide to form the corresponding 2-bromoimidazoles that were further functionalized using a Suzuki coupling reaction.
伯脲已被用作铑催化的与一系列重氮羰基化合物的N-H插入反应的底物。该插入反应高效,具有出色的选择性和产率。与重氮酮发生插入反应生成的产物在酸存在下容易环化,生成相应的咪唑酮,这些咪唑酮可通过与烷基、烯丙基和苄基卤化物进行N-烷基化进一步衍生化。或者,将咪唑酮用氧溴化磷处理以形成相应的2-溴咪唑,然后使用铃木偶联反应对其进行进一步官能化。