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Nickel-Catalyzed Regio-and Stereoselective Defluorinative Arylation of gem-Difluorinated Cyclopropanes
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作者 Shutao Qi Yunkai Hua +2 位作者 Liangkai Pan Junfeng Yang Junliang Zhang 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2024年第8期823-828,共6页
Comprehensive Summary,Herein,we report nickel-catalyzed cross-coupling of gem-difluorinated cyclopropanes with boronic acids,providing the corresponding arylated 2-fluoroallylic scaffolds.This approach used commercial... Comprehensive Summary,Herein,we report nickel-catalyzed cross-coupling of gem-difluorinated cyclopropanes with boronic acids,providing the corresponding arylated 2-fluoroallylic scaffolds.This approach used commercially available phosphine ligand Xantphos to obtain monofluorinated alkenes with high regioselectivity and Z-stereoselectivity.Mechanistic studies proposed a Ni(II)-fluoroallyl pathway and excluded the radical pathway. 展开更多
关键词 Nickel Monofluoroolefin CYCLOPROPANE Regioselectivity STEREOSELECTIVITY C-C coupling Cross-coupling Synthetic methods
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