Bond-forming and-breaking reactions at sulfur (IV): sulfoxides, sulfonium salts, sulfur ylides, and sulfinate salts

D Kaiser, I Klose, R Oost, J Neuhaus… - Chemical …, 2019 - ACS Publications
Organosulfur compounds have long played a vital role in organic chemistry and in the
development of novel chemical structures and architectures. Prominent among these …

Radicals: reactive intermediates with translational potential

M Yan, JC Lo, JT Edwards… - Journal of the American …, 2016 - ACS Publications
This Perspective illustrates the defining characteristics of free radical chemistry, beginning
with its rich and storied history. Studies from our laboratory are discussed along with recent …

Carbon trifluoromethylation reactions of hydrocarbon derivatives and heteroarenes

C Alonso, E Martinez de Marigorta, G Rubiales… - Chemical …, 2015 - ACS Publications
Fluorine has emerged as a “magic element” in medicinal chemistry, crop, and materials
science. 1 Although fluorine is the most abundant halogen in the earth's crust, it is contained …

Good partnership between sulfur and fluorine: sulfur-based fluorination and fluoroalkylation reagents for organic synthesis

C Ni, M Hu, J Hu - Chemical Reviews, 2015 - ACS Publications
Fluorine, often called as “a small atom with a big ego”, 1 lies in the second row and the 17th
column in the periodic table of the chemical elements. This unique position in the periodic …

Application of Langlois' reagent in trifluoromethylation reactions

C Zhang - Advanced Synthesis & Catalysis, 2014 - Wiley Online Library
The incorporation of a trifluoromethyl (CF3) group into organic compounds is of great
importance in pharmaceutical, agricultural, and materials science. Trifluoromethylation …

Pushing the boundaries of C–H bond functionalization chemistry using flow technology

S Govaerts, A Nyuchev, T Noel - Journal of Flow Chemistry, 2020 - Springer
C–H functionalization chemistry is one of the most vibrant research areas within synthetic
organic chemistry. While most researchers focus on the development of small-scale batch …

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

H Guyon, H Chachignon… - Beilstein Journal of …, 2017 - beilstein-journals.org
Abstract Sodium trifluoromethanesulfinate, CF 3 SO 2 Na, and trifluoromethanesulfonyl
chloride, CF 3 SO 2 Cl, are two popular reagents that are widely used for the direct …

Distinct mechanism of oxidative trifluoromethylation with a well-defined Cu (II) fluoride promoter: hidden catalysis

N Nebra, VV Grushin - Journal of the American Chemical Society, 2014 - ACS Publications
The fluoride [(bpy) CuF2 (H2O)]· 2H2O (1) reacts with CF3SiMe3 and PhB (OH) 2 in DMF at
rt to give PhCF3 in> 95% yield within 15 min. Although 1 is a Cu (II) complex, this reaction …

Advances in metal-assisted non-electrophilic fluoroalkylation reactions of organic compounds

B Lantano, MR Torviso, SM Bonesi… - Coordination Chemistry …, 2015 - Elsevier
Metal-assisted trifluoromethylation and perfluoroalkylation reactions are probably one of the
first approaches employed to achieve fluoroalkyl-group substitutions of organic substrates …

Copper-catalysed ring-opening trifluoromethylation of cyclopropanols

XP He, YJ Shu, JJ Dai, WM Zhang, YS Feng… - Organic & Biomolecular …, 2015 - pubs.rsc.org
A copper-catalysed ring-opening trifluoromethylation reaction of cyclopropanols has been
developed. Various β-trifluoromethyl ketones are obtained in good to excellent yields under …