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Journal ArticleDOI

Trifluoroacetic acid: Uses and recent applications in organic synthesis

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TLDR
Trifluoroacetic acid (TFA) has been widely used in organic synthesis as a solvent, catalyst and reagent as discussed by the authors, including rearrangements, functional group deprotections, oxidations, reductions, condensations, hydroarylations and trifluoromethylations.
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This article is published in Journal of Fluorine Chemistry.The article was published on 2013-12-01. It has received 63 citations till now. The article focuses on the topics: Trifluoroacetic acid & Organic synthesis.

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Where Does the Fluorine Come From? A Review on the Challenges Associated with the Synthesis of Organofluorine Compounds

TL;DR: In this article, the supply chain to access the necessary raw materials, which is critical for a variety of applications, including pharmaceutical products, is discussed. And the authors propose a solution to this problem.
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Multimedia Distribution and Transfer of Per- and Polyfluoroalkyl Substances (PFASs) Surrounding Two Fluorochemical Manufacturing Facilities in Fuxin, China.

TL;DR: The concentrations of individual PFASs in air, outdoor settled dust, and surface river water decreased exponentially as the distance increases from the FMPs, whereas the concentrations of short-chain perfluoroalkyl carboxylic acids (PFCAs) remained high in the surface water 38 km away.
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Silver-catalyzed C-H trifluoromethylation of arenes using trifluoroacetic acid as the trifluoromethylating reagent.

TL;DR: This reaction not only provides a new protocol for aryl C-H trifluoromethylation, but the generation of CF3· from TFA may prove useful in other contexts and could potentially be extended to other triffluorometHylation reactions.
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A novel process for recycling and resynthesizing LiNi1/3Co1/3Mn1/3O2 from the cathode scraps intended for lithium-ion batteries.

TL;DR: Electrochemical tests show that the initial charge and discharge capacities of the resynthesized LiNi1/3Co 1/3Mn1/ 3O2 are 201 mAh g(-)(1) and 155.4 m Ah g(-1) (2.8-4.5 V, 0.1C), respectively.
References
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Journal ArticleDOI

Lyotropic mesomorphic formation of cellulose in trifluoroacetic acid-chlorinated-alkane solvent mixtures at room temperature

TL;DR: In this article, trifluoroacetic acid (TFA)-1, 2-dichloroethane (1,2-DCE), TFA-Dichloromethane (CH2Cl2), and TFA trichlorometric acid (CHCl3) solvents were used to obtain lyotropic cellulose mesophases.
Book

Ionic and Organometallic-Catalyzed Organosilane Reductions

TL;DR: Larson and Fry as discussed by the authors proposed an adjective and adjective-and-allic-catalyzed ORGANOSILANE REDUCTIONS (Gerald L. Larson and James L. Fry, 2003).
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Mg-promoted double silylation of trifluoroacetimidoyl chlorides. A new entry to the fluorinated dianion equivalents.

TL;DR: A Mg(0)/Me(3)SiCl system was found to be effective for the preparation of a novel fluorinated dianion equivalent and a one-pot reaction sequence involving reductive C-F and C-Cl bond cleavage reactions of trifluoroacetimidoyl chlorides afforded bis-silylated difluoroenamines.
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