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Synthesis of CF3-Substituted 1,6-Dihydropyridazines by Copper-Promoted Cascade Oxidation/Cyclization of Trifluoromethylated Homoallylic N-Acylhydrazines.
The Journal of Organic Chemistry ( IF 3.3 ) Pub Date : 2020-09-03 , DOI: 10.1021/acs.joc.0c01568 Tianyu Yang 1 , Zhoubin Deng 1 , Ke-Hu Wang 1 , Pengfei Li 1 , Danfeng Huang 1 , Yingpeng Su 1 , Yulai Hu 1, 2
The Journal of Organic Chemistry ( IF 3.3 ) Pub Date : 2020-09-03 , DOI: 10.1021/acs.joc.0c01568 Tianyu Yang 1 , Zhoubin Deng 1 , Ke-Hu Wang 1 , Pengfei Li 1 , Danfeng Huang 1 , Yingpeng Su 1 , Yulai Hu 1, 2
Affiliation
A highly efficient strategy for the construction of CF3-substituted 1,6-dihydropyridazines has been developed by cascade oxidation/cyclization of trifluoromethylated N-acylhydrazines. The produced 1,6-dihydropyridazines could be easily transformed to 3-trifluoromethyl pyridazine derivatives. Some of the 1,6-dihydropyridazines exhibited aggregation-induced emission (AIE). DFT calculations were conducted to explain the mechanism.
中文翻译:
三氟甲基化均烯丙基N-酰基肼的铜促进的级联氧化/环化反应合成CF3取代的1,6-二氢哒嗪。
通过三氟甲基化的N-酰基肼的级联氧化/环化,已经开发出一种构造CF 3-取代的1,6-二氢哒嗪的高效策略。产生的1,6-二氢哒嗪可以很容易地转化为3-三氟甲基哒嗪衍生物。一些1,6-二氢哒嗪显示出聚集诱导的发射(AIE)。进行了DFT计算以解释该机理。
更新日期:2020-10-02
中文翻译:
三氟甲基化均烯丙基N-酰基肼的铜促进的级联氧化/环化反应合成CF3取代的1,6-二氢哒嗪。
通过三氟甲基化的N-酰基肼的级联氧化/环化,已经开发出一种构造CF 3-取代的1,6-二氢哒嗪的高效策略。产生的1,6-二氢哒嗪可以很容易地转化为3-三氟甲基哒嗪衍生物。一些1,6-二氢哒嗪显示出聚集诱导的发射(AIE)。进行了DFT计算以解释该机理。