Results 11 to 20 of about 3,603 (218)

Progress in copper-catalyzed trifluoromethylation

open access: yesBeilstein Journal of Organic Chemistry, 2018
The introduction of trifluoromethyl groups into organic molecules has attracted great attention in the past five years. In this review, we describe the recent efforts in the development of trifluoromethylation via copper catalysis using nucleophilic ...
Guan-bao Li   +3 more
doaj   +2 more sources

Trifluoromethylation of graphene

open access: yesAPL Materials, 2014
We demonstrate trifluoromethylation of graphene by copper-catalyzed free radical reaction. The covalent addition of CF3 to graphene, which changes the carbon atom hybridization from sp2 to sp3, and modifies graphene in a homogeneous and nondestructive ...
Lin Zhou   +7 more
doaj   +2 more sources

Photocatalytic Activation of Fluoroform for Radical Trifluoromethylation. [PDF]

open access: yesJ Am Chem Soc
Fluoroform is an ideal trifluoromethyl source in synthetic chemistry due to its low cost, low toxicity, and high potential for greenhouse-gas valorization.
Zhou S   +9 more
europepmc   +2 more sources

3-Position-Selective C–H Trifluoromethylation of Pyridine Rings Based on Nucleophilic Activation [PDF]

open access: yes, 2022
The first example of the 3-position-selective C(sp2)–H trifluoromethylation of pyridine rings was established. 3-Position-selective trifluoromethylation was achieved by the nucleophilic activation of pyridine and quinoline derivatives through ...
Yoichiro, Kuninobu   +2 more
core   +3 more sources

Redox-Neutral Decarboxylative and Desulfonylative C(sp3) Trifluoromethylation: Method Development and Mechanistic Inquiry [PDF]

open access: yes, 2023
Sodium triflinate (CF3SO2Na) is an inexpensive bench stable radical CF3 source that is often activated by external oxidants such as peroxides. However, despite the commercial accessibility of CF3SO2Na, the salt has never been applied to decarboxylative ...
Chris, Seong, Courtney, Roberts
core   +2 more sources

Regioselective C–H Trifluoromethylation of Aromatic Compounds by Inclusion in Cyclodextrins [PDF]

open access: yes, 2021
A regioselective radical C–H trifluoromethylation of aromatic compounds was developed using cyclodextrins (CDs) as additives. The C–H trifluoromethylation proceeded with high regioselectivity to afford the product in good yield, even on the gram scale ...
Jizhou, Song   +5 more
core   +2 more sources

Site-specific Deaminative Trifluoromethylation of Aliphatic Primary Amines [PDF]

open access: yes, 2023
The introduction of trifluoromethyl groups into organic molecules is of paramount importance in modern synthetic chemistry and medicinal chemistry. While methods for constructing C(sp2)-CF3 bonds have been well established, the advancement of practical ...
Yin , Li   +4 more
core   +2 more sources

Commercial-Scale Visible-light Trifluoromethylation of 2-Chlorothiophenol using CF3I gas. [PDF]

open access: yes, 2021
Despite the growth of photoredox methods in academia, application of photoredox at scale in the pharmaceutical and fine chemical industries has been slow.
Ping-zhong, Huang   +15 more
core   +2 more sources

Rapid Biomolecular Trifluoromethylation Using Cationic Aromatic Sulfonate Esters as Visible Light-Triggered Radical Photocages [PDF]

open access: yes, 2023
Described here is a photo-decaging approach to radical trifluoromethylation of biomolecules. This was accomplished by designing a quinolinium sulfonate ester that, upon absorption of visible light, achieves decaging via photolysis of the sulfonate ester
Michael, Taylor, Nicholas, Kuehl
core   +2 more sources

Cs2CO3-Initiated Trifluoro-Methylation of Chalcones and Ketones for Practical Synthesis of Trifluoromethylated Tertiary Silyl Ethers

open access: yesMolecules, 2017
It was found that 1,2-trifluoromethylation reactions of ketones, enones, and aldehydes were easily accomplished using the Prakash reagent in the presence of catalytic amounts of cesium carbonate, which represents an experimentally convenient, atom ...
Cheng Dong   +6 more
doaj   +1 more source

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