Activation of trifluoromethyltrimethylsilane by potassium fluoride in N,N-dimethylacetamide provides a powerful source of trifluoromethide which is capable of substituting aromatic nitro and cyano groups under nucleophilic conditions, albeit in low yield. The trifluoromethide generated in this system is also a potent base which leads to a number of interesting side reactions via deprotonation of the substrate
Trifluorodiazoethane (CF3CHN2), a highly reactive fluoroalkylating reagent, offers a useful means to...
This thesis is concerned with the development of methodology for late-stage trifluoromethylation of ...
Using a commercially available Umemoto’s reagent, the metal-free trifluoromethylation of nitroalkane...
Nucleophilic routes to selectively fluorinated aromatic compounds starting from cheap and readily av...
Organofluorine compounds exhibit biological activity and have advantageous properties for drug desig...
A means to trifluoromethylate: The beneficial properties imparted by the trifluoromethylation of aro...
A novel strategy for aromatic trifluoromethylation by converting aromatic amino group into CF3 group...
The trifluoromethylation of aryl/heteroaryl iodides has been demonstrated using a flow system, enabl...
International audienceDirect trifluoromethylthiolation of various aromatic and heteroaromatic compou...
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
98 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1984.Trifluoroacetyl triflate is re...
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
Incorporation of fluorine atoms into organic molecules significantly enhances many of their properti...
Within the past few decades, the presence of fluorine containing organic molecules has increased sig...
The trifluoromethyl group involved in organic compounds plays important roles as a key functional gr...
Trifluorodiazoethane (CF3CHN2), a highly reactive fluoroalkylating reagent, offers a useful means to...
This thesis is concerned with the development of methodology for late-stage trifluoromethylation of ...
Using a commercially available Umemoto’s reagent, the metal-free trifluoromethylation of nitroalkane...
Nucleophilic routes to selectively fluorinated aromatic compounds starting from cheap and readily av...
Organofluorine compounds exhibit biological activity and have advantageous properties for drug desig...
A means to trifluoromethylate: The beneficial properties imparted by the trifluoromethylation of aro...
A novel strategy for aromatic trifluoromethylation by converting aromatic amino group into CF3 group...
The trifluoromethylation of aryl/heteroaryl iodides has been demonstrated using a flow system, enabl...
International audienceDirect trifluoromethylthiolation of various aromatic and heteroaromatic compou...
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
98 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1984.Trifluoroacetyl triflate is re...
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
Incorporation of fluorine atoms into organic molecules significantly enhances many of their properti...
Within the past few decades, the presence of fluorine containing organic molecules has increased sig...
The trifluoromethyl group involved in organic compounds plays important roles as a key functional gr...
Trifluorodiazoethane (CF3CHN2), a highly reactive fluoroalkylating reagent, offers a useful means to...
This thesis is concerned with the development of methodology for late-stage trifluoromethylation of ...
Using a commercially available Umemoto’s reagent, the metal-free trifluoromethylation of nitroalkane...