Advances in the Synthesis of Fluorinated Scaffolds by Transition Metal-Catalyzed C-H Bond Activation

被引:2
|
作者
Mazeh, Sara [1 ]
Lapuh, Maria Ivana [1 ]
Besset, Tatiana [1 ]
机构
[1] Normandie Univ, INSA Rouen, UNIROUEN, CNRS,COBRA UMR 6014, F-76000 Rouen, France
基金
欧洲研究理事会;
关键词
C-H bond functionalization; Emergent fluorinated groups; Organofluorine chemistry; Synthetic methods; Transition metal; ALPHA-TRIFLUOROMETHYLSTYRENE DERIVATIVES; UNACTIVATED C(SP(3))-H BONDS; HYPERVALENT IODONIUM YLIDE; BORONIC ACIDS; DIRECT TRIFLUOROMETHYLTHIOLATION; ELECTROPHILIC TRIFLUOROMETHYLTHIOLATION; SILVER(I) TRIFLUOROMETHANETHIOLATE; OLEFINIC TRIFLUOROMETHYLATION; STEREOSELECTIVE-SYNTHESIS; SUBSTITUENT CONSTANTS;
D O I
10.2533/chimia.2020.871
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Thanks to the unique features of the fluorine atom and the fluorinated groups, fluorine-containing molecules are essential. Therefore, the search for new fluorinated groups as well as straightforward and original methodologies for their installation is of prime importance. Especially, the combination of organofluorine chemistry with transition metal-catalyzed C-H bond functionalization reactions offered straightforward tools to access original fluorinated scaffolds. In this context, over the last years, our group focused on the development of original methodologies to synthesize fluorine-containing molecules with a special attention to emergent fluorinated groups. The present account highlights our recent contributions to the synthesis of highly value-added fluorine-containing compounds by transition metal-catalyzed C-H bond activation.
引用
收藏
页码:871 / 877
页数:7
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