Shindoh Naoya, Tokuyama Hidetoshi, Takemoto Yoshiji, Takasu Kiyosei
Graduate School of Pharmaceutical Sciences, Kyoto University, Yoshida, Sakyo-ku, Kyoto 606-8501, Japan.
J Org Chem. 2008 Oct 3;73(19):7451-6. doi: 10.1021/jo8009243. Epub 2008 Aug 30.
We demonstrated a catalytic cascade inverse electron demand hetero-Diels-Alder reaction (Povarov reaction) and hydrogen-transfer process. The reaction of electron-rich olefins and excess amount of imines in the presence of acid catalysts under appropriate conditions affords substituted quinolines in a single operation. In the cascade process, the catalysts, such as Tf2NH, TfOH, and Lewis acids, catalyze two mechanistically distinct reactions (auto-tandem catalysis). We also describe the synthetic utility of the prepared quinolines.
我们展示了一个催化级联逆电子需求杂环狄尔斯-阿尔德反应(波瓦罗夫反应)和氢转移过程。在适当条件下,富电子烯烃与过量亚胺在酸催化剂存在下反应,可一步合成取代喹啉。在级联过程中,诸如双(三氟甲磺酰)亚胺、三氟甲磺酸和路易斯酸等催化剂催化两个机理不同的反应(自动串联催化)。我们还描述了所制备喹啉的合成效用。