Results 1 to 10 of about 1,330 (177)
Catalytic trifluoromethylation of iodoarenes by use of 2-trifluoromethylated benzimidazoline as trifluoromethylating reagent [PDF]
The trifluoromethylation of iodoarenes was accomplished by use of a 2-trifluoromethylbenzimidazoline derivative as the trifluoromethylating reagent and a catalytic amount of Cu(I) in the presence of 2,2'-bipyridyl as the ligand.
Tatsuhiro Uchikura +3 more
doaj +3 more sources
Dual-role iron species in photoelectrocatalytic radical trifluoromethylation with trifluoroacetates [PDF]
Trifluoromethylation remains a fundamental transformation in drug discovery, underpinning many top-selling pharmaceuticals. Emerging developments in iron ligand-to-metal charge transfer (LMCT) catalysis have redefined fluoroalkylation chemistry by ...
Sara Fernández-García +4 more
doaj +2 more sources
Advances in photocatalytic research on decarboxylative trifluoromethylation of trifluoroacetic acid and derivatives [PDF]
Trifluoromethylation stands as a pivotal technology in modern synthetic chemistry, playing an indispensable role in drug design, functional material development, and agrochemical innovation.
Fang-Fang Tan +3 more
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Copper-catalyzed trifluoromethylation of alkenes with an electrophilic trifluoromethylating reagent [PDF]
An efficient method for the copper-catalyzed trifluoromethylation of terminal alkenes with an electrophilic trifluoromethylating reagent has been developed. The reactions proceeded smoothly to give trifluoromethylated alkenes in good to excellent yields.
Xiao-Ping Wang +4 more
doaj +3 more sources
Photoorganocatalytic trifluoromethylation of (het)arenes in green conditions [PDF]
A sustainable photocatalytic protocol for the trifluoromethylation of (hetero)arenes is reported. The method operates under metal- and base-free conditions using an inexpensive and atom-efficient CF3 source, trifluoroacetic anhydride, in ethyl acetate as
Egor N. Boronin +8 more
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Copper-Catalyzed Trifluoromethylation of Alkoxypyridine Derivatives
The trifluoromethylation of aromatic and heteroaromatic cores has attracted considerable interest in recent years due to its pharmacological relevance.
Nandor Gyorfi +5 more
doaj +1 more source
A straightforward method that enables the formation of biologically attractive trifluoromethyl ketones from readily available methyl esters using the potent greenhouse gas fluoroform (HCF3, HFC-23) was developed.
Yamato Fujihira +5 more
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Synthesis of Trifluoromethylated Monoterpene Amino Alcohols
For the first time, monoterpene trifluoromethylated β-hydroxy-benzyl-O-oximes were synthesized in 81–95% yields by nucleophilic addition of the Ruppert–Prakash reagent (TMSCF3) to the corresponding β-keto-benzyl-O-oximes based on (+)-nopinone ...
Polina A. Petrova +5 more
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Activation of SF5CF3 by the N-Heterocyclic Carbene SIMes
The greenhouse gas SF5CF3 was photochemically activated with SIMes (1,3-Bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidene) to give 1,3-dimesityl-2,2-difluoroimidazolidine (SIMesF2), and 1,3-dimesitylimidazolidine-2-sulfide, as well as the ...
Domenique Herbstritt +2 more
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Summary: Trifluoroacetic acid (TFA) is among the most attractive trifluoromethylation reagents with respect to its low prices, ease of handling, and availability in large quantities.
Dehang Yin, Dengquan Su, Jian Jin
doaj +1 more source

