Results 61 to 70 of about 1,340 (176)
Photocatalytic fluoroalkylation by ligand-to-metal charge transfer
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
THE RADICAL C-H FUNCTIONALIZATION OF NATURAL COMPOUNDS
Selective functionalization of complex scaffolds is a promising approach to increase the pharmacological profiles of natural products and their derivatives.
Vladilena GÎRBU
doaj
Shelf-stable electrophilic trifluoromethylating reagents: A brief historical perspective
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
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
This short review highlights the copper-mediated fluoroalkylation using perfluoroalkylated carboxylic acid derivatives. Carbon–carbon bond cleavage of perfluoroalkylated carboxylic acid derivatives takes place in fluoroalkylation reactions at high ...
Tsuyuka Sugiishi +3 more
doaj +1 more source
The recent progresses of the application of trifluoromethanesulfonyl chloride, CF3SO2Cl, in the formation of C–CF3, C–SCF3, C–SOCF3, and C–Cl bonds are summarised in this second part of a two-part review published back-to-back on both sodium ...
Hélène Chachignon +2 more
doaj +1 more source
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
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
K. Anusha +4 more
doaj +1 more source
Trifluoromethylation of pyridines through skeletal rearrangement. [PDF]
Wang H, Bhaduri N, Greaney MF.
europepmc +1 more source

