Results 31 to 40 of about 3,603 (218)

High-Valent NiIII and NiIV Species Relevant to C–C and C–Heteroatom Cross-Coupling Reactions: State of the Art

open access: yesMolecules, 2020
Ni catalysis constitutes an active research arena with notable applications in diverse fields. By analogy with its parent element palladium, Ni catalysts provide an appealing entry to build molecular complexity via cross-coupling reactions.
Noel Nebra
doaj   +1 more source

Cu-Mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3

open access: yesBeilstein Journal of Organic Chemistry, 2013
A Cu-mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3 was developed for the first time. This method offers a convenient and economical approach to various trifluoroethyl-containing compounds.
Xueliang Jiang, Feng-Ling Qing
doaj   +1 more source

Biocatalytic trifluoromethylation of unprotected phenols

open access: yesNature Communications, 2016
The introduction of fluorine into organic molecules often requires prefunctionalised molecules or protection of reactive functional groups. Here, the authors report a biocatalytic method for the trifluoromethylation of unprotected phenols under mild ...
Robert C. Simon   +5 more
doaj   +1 more source

Iron(II)-catalyzed trifluoromethylation of vinylcyclopropanes

open access: yes上海师范大学学报. 自然科学版, 2016
An efficient iron(II)-catalyzed trifluoromethylation of vinylcyclopropanes was developed.A series of CF3-containing dihydronaphthalene derivatives were prepared with a moderate to high yield.This method offers several advantages in terms of its mild ...
LI Zongrui, DENG Qinghai
doaj   +1 more source

Recent Advances in Trifluoromethylation Reactions with Electrophilic Trifluoromethylating Reagents

open access: yesChemistry – A European Journal, 2014
Abstract Electrophilic trifluoromethylation reactions have been the latest approach to achieve the fluoroalkylation of compounds with newly‐discovered reagents, such as the Togni’s (1‐trifluoromethyl‐1,2‐benziodoxol‐3‐(1 H)‐one), Umemoto’s (S‐(trifluoromethyl)dibenzothiophenium tetrafluoroborate), Yagupolskii’s (S‐
Barata Vallejo, Sebastian   +2 more
openaire   +3 more sources

CF3SO2X (X = Na, Cl) as reagents for trifluoromethylation, trifluoromethylsulfenyl-, -sulfinyl- and -sulfonylation. Part 1: Use of CF3SO2Na

open access: yesBeilstein Journal of Organic Chemistry, 2017
Sodium trifluoromethanesulfinate, CF3SO2Na, and trifluoromethanesulfonyl chloride, CF3SO2Cl, are two popular reagents that are widely used for the direct trifluoromethylation of a large range of substrates.
Hélène Guyon   +2 more
doaj   +1 more source

Pd/C‐Catalyzed Hydrogenation of CF3‐, CF2H‐, and CF2CO2Et‐containing Pyridines: A Robust Method for Highly Functionalized containing Piperidines

open access: yesAngewandte Chemie, Volume 138, Issue 34, 17 August 2026.
A robust and efficient method to access diversely functionalized fluorinated piperidines was developed. The approach features the hydrogenation of polysubstituted pyridines bearing CF3, CF2H, and CF2CO2Et substituents using an inexpensive, readily available heterogeneous Pd/C catalyst under air‐ and moisture‐tolerant conditions, offering an appealing ...
Thibaud Charvillat   +7 more
wiley   +2 more sources

Copper-Catalyzed Decarboxylative Trifluoromethylation Reactions [PDF]

open access: yes, 2017
Trifluoromethanes play an important role in medicinal chemistry, and methods that enable the rapid synthesis of trifluoromethanes from common functional groups are essential for the synthesis of bioactive compounds.
Ambler, Brett R.
core   +1 more source

Regioselective 1,4-trifluoromethylation of α,β-unsaturated ketones via a S-(trifluoromethyl)diphenylsulfonium salts/copper system

open access: yesBeilstein Journal of Organic Chemistry, 2013
Regioselective conjugate 1,4-trifluoromethylation of α,β-unsaturated ketones by the use of shelf-stable electrophilic trifluoromethylating reagents, S-(trifluoromethyl)diphenylsulfonium salts and copper under mild conditions is described. A wide range of
Satoshi Okusu   +3 more
doaj   +1 more source

Electron Donor–Acceptor Complex Catalysis in Synthetic Chemistry

open access: yesAngewandte Chemie International Edition, EarlyView.
Electron donor–acceptor (EDA) complexes are moving beyond stoichiometric photoactivation toward catalytic platforms for radical generation. Productive EDA catalysis requires coordinated donor–acceptor association, charge‐transfer excitation, radical reactivity, and vcatalyst turnover.
Tristan von Münchow   +3 more
wiley   +1 more source

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