Results 61 to 70 of about 1,330 (177)

Determining the predominant tautomeric structure of iodine-based group-transfer reagents by 17O NMR spectroscopy

open access: yesBeilstein Journal of Organic Chemistry, 2018
Cyclic benziodoxole systems have become a premier scaffold for the design of electrophilic transfer reagents. A particularly intriguing aspect is the fundamental II–IIII tautomerism about the hypervalent bond, which has led in certain cases to a ...
Nico Santschi   +3 more
doaj   +1 more source

Recent advances in transition metal-catalyzed Csp2-monofluoro-, difluoro-, perfluoromethylation and trifluoromethylthiolation

open access: yesBeilstein Journal of Organic Chemistry, 2013
In the last few years, transition metal-mediated reactions have joined the toolbox of chemists working in the field of fluorination for Life-Science oriented research.
Grégory Landelle   +4 more
doaj   +1 more source

Photocatalytic fluoroalkylation by ligand-to-metal charge transfer

open access: yesFrontiers in Chemistry
Trifluoromethyl (CF3) and other fluoroalkyl groups are of great significance in the fields of pharmaceutical chemistry and agricultural chemicals. Fluoroalkyl acids, especially trifluoroacetic acid (TFA) is considered the most ideal fluoroalkylation ...
Jingyi Liu   +6 more
doaj   +1 more source

Shelf-stable electrophilic trifluoromethylating reagents: A brief historical perspective

open access: yesBeilstein Journal of Organic Chemistry, 2010
Since the discovery by Yagupolskii and co-workers that S-trifluoromethyl diarylsulfonium salts are effective for the trifluoromethylation of thiophenolates, the design and synthesis of electrophilic trifluoromethylating reagents have been extensively ...
Norio Shibata   +2 more
doaj   +1 more source

Copper-catalyzed remote C(sp 3)–H azidation and oxidative trifluoromethylation of benzohydrazides

open access: yesNature Communications, 2019
Functionalization of carbon radicals formed via 1,5-hydrogen atom transfer of amidyl radicals is an underdeveloped protocol for remote C–H functionalization.
Xu Bao, Qian Wang, Jieping Zhu
doaj   +1 more source

THE RADICAL C-H FUNCTIONALIZATION OF NATURAL COMPOUNDS

open access: yesStudia Universitatis Moldaviae: Stiinte reale si ale naturii, 2019
Selective functionalization of complex scaffolds is a promising approach to increase the pharmacological profiles of natural products and their derivatives.
Vladilena GÎRBU
doaj  

1,6-Nucleophilic Di- and Trifluoromethylation of para-Quinone Methides with Me3SiCF2H/Me3SiCF3 Facilitated by CsF/18-Crown-6

open access: yesMolecules
The direct 1,6-nucleophilic difluoromethylation, trifluoromethylation, and difluoroalkylation of para-quinone methides (p-QMs) with Me3SiRf (Rf = CF2H, CF3, CF2CF3, CF2COOEt, and CF2SPh) under mild conditions are described. Although Me3SiCF2H shows lower
Dingben Chen   +7 more
doaj   +1 more source

1,2-Oxidative Trifluoromethylation of Olefin with Ag(O2CCF2SO2F) and O2: Synthesis of α-Trifluoromethyl Ketones

open access: yesMolecules
A novel and efficient 1,2-oxidative trifluoromethylation of olefins employing Ag(O2CCF2SO2F) as a trifluoromethyl source is described with O2 as the oxidant, which provides access to a variety of valuable α-trifluoromethyl-substituted ketones.
Shengxue Zhang   +7 more
doaj   +1 more source

Visible-light-induced radical cascade cyclization: a catalyst-free synthetic approach to trifluoromethylated heterocycles

open access: yesBeilstein Journal of Organic Chemistry
A visible-light-promoted research protocol for constructing dihydropyrido[1,2-a]indolone skeletons is herein described proceeding through a cascade cyclization mediated by trifluoromethyl radicals.
Chuan Yang   +5 more
doaj   +1 more source

Langlois Reagent: An Efficient Trifluoromethylation Reagent

open access: yesSynOpen, 2023
K. Anusha   +4 more
doaj   +1 more source

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