Silver-Catalyzed Radical Phosphonofluorination of Unactivated Alkenes
摘要:
We report herein a mild and catalytic phosphonofluorination of unactivated alkenes. With catalysis by AgNO3, the condensation of various unactivated alkenes with diethyl phosphite and Selectfluor reagent in CH2Cl2/H2O/HOAc at 40 degrees C led to the efficient synthesis of beta-fluorinated alkylphosphonates with good stereoselectivity and wide functional group compatibility. A mechanism involving silver-catalyzed oxidative generation of phosphonyl radicals and silver-assisted fluorine atom transfer is proposed.
Free-radical anti-Markovnikov hydroalkylation of unactivated alkenes with simple alkanes
作者:Yunfei Tian、Anbo Ling、Ren Fang、Ren Xiang Tan、Zhong-Quan Liu
DOI:10.1039/c8gc01394b
日期:——
A Cu(II)-mediated radical anti-Markovnikov hydroalkylation of unactivated alkenes with simple alkanes via selective C(sp3)–Hbond cleavage was achieved. This reaction features high site-selectivity diverse functional group tolerance, and scalability.
Silver-Catalyzed Radical Phosphonofluorination of Unactivated Alkenes
作者:Chengwei Zhang、Zhaodong Li、Lin Zhu、Limei Yu、Zhentao Wang、Chaozhong Li
DOI:10.1021/ja408031s
日期:2013.9.25
We report herein a mild and catalytic phosphonofluorination of unactivated alkenes. With catalysis by AgNO3, the condensation of various unactivated alkenes with diethyl phosphite and Selectfluor reagent in CH2Cl2/H2O/HOAc at 40 degrees C led to the efficient synthesis of beta-fluorinated alkylphosphonates with good stereoselectivity and wide functional group compatibility. A mechanism involving silver-catalyzed oxidative generation of phosphonyl radicals and silver-assisted fluorine atom transfer is proposed.