An approach for the synthesis of quinolizinone with potential bioactivity has been developed via palladium-catalytic dearomative cyclocarbonylation of allyl alcohol. Diverse quinolizinone compounds could be attained with good efficiencies. A feasible reaction pathway could be a successive procedure of allylation, dearomatization, CO insertion and the Heck reaction.
通过
钯催化
烯丙醇的脱芳香环羰基化,已经开发了一种具有潜在
生物活性的
喹喔啉酮合成方法。可以高效获得各种
喹啉嗪酮化合物。可行的反应途径可以是烯丙基化,脱芳香化,CO插入和Heck反应的连续过程。