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Access to Ketones via Nickel-Catalyzed Coupling between S-2-Pyridyl Thioesters and Redox-Active Esters Using an Organic Reductant
The Journal of Organic Chemistry ( IF 3.3 ) Pub Date : 2024-11-15 , DOI: 10.1021/acs.joc.4c01242 Jiang-Hong Liu, Ze-Yu Tian, Zhen-Ye Wu, Tian-Le Huang, Zheng Lin, Le Zhang, Jian Chen, Li Hai, Li Guo, Yong Wu
The Journal of Organic Chemistry ( IF 3.3 ) Pub Date : 2024-11-15 , DOI: 10.1021/acs.joc.4c01242 Jiang-Hong Liu, Ze-Yu Tian, Zhen-Ye Wu, Tian-Le Huang, Zheng Lin, Le Zhang, Jian Chen, Li Hai, Li Guo, Yong Wu
A nickel-catalyzed coupling between S-2-pyridyl thioesters and redox-active esters has been reported. Diludine was used as a reductant in this strategy. Our method rapidly achieves the target ketone products in moderate to good yield. The construction of nonanomeric C-acyl glycosides was realized through the approach as well.
中文翻译:
使用有机还原剂通过 S-2-吡啶基硫酯和氧化还原活性酯之间的镍催化偶联获得酮
据报道,S-2-吡啶硫酯和氧化还原活性酯之间存在镍催化偶联。Diludine 在该策略中用作还原剂。我们的方法以中等到良好的收率快速获得目标酮产物。九异体 C-酰基糖苷的构建也是通过该方法实现的。
更新日期:2024-11-15
中文翻译:
使用有机还原剂通过 S-2-吡啶基硫酯和氧化还原活性酯之间的镍催化偶联获得酮
据报道,S-2-吡啶硫酯和氧化还原活性酯之间存在镍催化偶联。Diludine 在该策略中用作还原剂。我们的方法以中等到良好的收率快速获得目标酮产物。九异体 C-酰基糖苷的构建也是通过该方法实现的。