A new bicyclization strategy has been established, allowing a flexible and practical approach to 33 examples of pyrazolo[3,4-c]quinolines from low-cost and readily accessible triethylammonium thiolates with hydrazines. Notably, the features of this work include broad functional group compatibility, mild reaction conditions and good reaction yields.
建立了一种新的双环化策略,可以采用灵活实用的方法从低成本且易于获得的
硫醇三乙
铵与
肼中合成 33 种
吡唑并[3,4- c ]
喹啉。值得注意的是,该工作的特点包括广泛的官能团兼容性、温和的反应条件和良好的反应产率。